Some 30 million people have sent their DNA to be analyzed by companies like 23andMe and AncestryDNA. But what happens once the sample is in the hands of testing companies, and how accurate are their results? NOVA explores the power of genetic data to reveal family connections, ancestry, and health risks—and even solve criminal cold cases. But alongside the benefits of these rapidly growing genetic databases are serious unintended consequences. (Premiered January 13, 2021)
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Secrets in our DNA
PBS Airdate: January 13, 2021
NARRATOR: A family secret exposed…
DANI SHAPIRO (Writer): If my father wasn’t my biological father, who was? Something very, very important was kept from me.
NARRATOR: …a hidden legacy revealed…
TYQUINE GOLDEN (Research Participant): Somewhere in slavery, that 20 percent might’ve been integrated with our DNA, and that might not have been voluntary.
NARRATOR: …a life-threatening illness prevented…
JESSICA ALGAZI (23andMe Customer): They quite possibly saved my life.
NARRATOR: …and a decades-old murder, finally solved…
CHELSEA RUSTAD (AncestryDNA Customer): Without my DNA, it would have been dead in the water.
NARRATOR: …just a few of the millions of stories launched by one of the most popular and promising new technologies, consumer DNA testing. With a swab or a bit of spit, some 30-million of us have turned over our most personal information, hoping to discover what’s hidden inside us.
But what do the tests really deliver?
LAVINIA ARSHID: Spain, Portugal, Norway?
NARRATOR: How good is the science? And how are the tests changing our lives?
JUNE SMITH (AncestryDNA Customer): I just couldn’t believe it. I was on the phone with my oldest sister.
NARRATOR: In search of clues, the Secrets in our DNA, right now, on NOVA.
It’s a promise many of us just can’t resist: send in your DNA and unlock secrets about family, ancestry and even health.
ANITA FOEMAN (West Chester University): It’s rare that something comes along that is truly new. And this is something that’s truly new.
NARRATOR: But just how reliable are consumer DNA tests and their scientific-looking ancestry percentages? Should we worry about our privacy? What are the unforeseen consequences, when we reveal the secrets in our DNA?
In the suburbs of Olympia, Washington, one woman finds out just how unpredictable those consequences can be.
Chelsea Rustad, who works as an I.T. specialist, is an avid family historian. In 2015, she takes a test with the biggest of the direct-to-consumer companies, AncestryDNA®.
CHELSEA RUSTAD: People end up doing it, oftentimes, because, “I just want to learn about my ancestral background.” But then something else pops up that they really were not expecting at all, and that’s exactly what this was for me.
NARRATOR: The test results suggest that Chelsea is mostly of Norwegian and German ancestry. Then, because she’s also curious to find new relatives, she downloads her raw file from Ancestry and uploads it to a free website called GEDmatch. It’s a place where anyone can search for matches, no matter what company they tested with.
GEDmatch shows Chelsea everyone else on the site who shares DNA with her.
CHELSEA RUSTAD: It’s kind of humbling and interesting to see those interconnections, to realize the sheer number of people that we share some percentage of DNA with and don’t even realize it.
NARRATOR: On GEDmatch, Chelsea sees an aunt whom she knows, but no new close relatives. She logs off, and doesn’t check the site again.
Three years go by. And then, on the evening of May 17, 2018, Chelsea gets some unexpected visitors.
CHELSEA RUSTAD: I looked through the peephole and, and see that there are two cops waiting outside there. And when I opened the door, they introduced themselves as investigators who are looking into a homicide that was a cold case from 31 years ago.
NARRATOR: They’ve come to her door as a result of that DNA file she posted on GEDmatch. To her amazement, they tell her that her DNA has led them to a suspect.
CHELSEA RUSTAD: It was just really a lot to take in and really shocking. Every step of what they explained to me is a horror story.
NARRATOR: Chelsea’s hopeful search for relatives has taken a dark turn, into the hunt for a killer, someone she’s related to.
Though her story is unusual, it shows that consumer DNA companies can fulfill one of their biggest promises extremely well: connecting us to our relatives.
Direct-to-consumer, or “D.T.C.” DNA testing, is a billion-dollar business, made possible by the simple rules of heredity.
CECE MOORE (Genetic Genealogist): We inherit our DNA from both of our parents: 50 percent from mom, 50 percent from dad. And they inherited it from their parents; and their parents, of course, inherited it from their parents.
NARRATOR: Our parents each contribute about 50 percent to our DNA. And the same is true for them and their parents. So, the amount of DNA we inherit from any ancestor drops by half with each preceding generation.
We also share DNA with anyone who shares a common ancestor with us: siblings, half-siblings, first cousins, second cousins and so on. The way that the D.T.C.s determine those relationships is by comparing people’s DNA. The amount that is shared is measured in a unit called centimorgans.
CECE MOORE: The more centimorgans two people share, the closer they are related. And the fewer centimorgans they share, the more distantly related they are.
NARRATOR: But with the D.T.C.s, a relationship to someone can’t always be determined just by counting centimorgans, because the numbers fall within ranges. You might share the same number with a cousin and a great-uncle, for example.
ELLEN GREYTAK (Parabon NanoLabs): Just because you have an amount of shared DNA doesn’t mean you actually know, for sure, what that person’s relationship is. It’s just a probability, a spectrum of possible relationships.
NARRATOR: June Smith lives in New Jersey, not far from Philadelphia. In 2018, she takes a consumer DNA test, hoping to solve a longstanding mystery. She’s spent years searching for her roots. When June was 16, growing up in Philadelphia, the woman she knew as her mother revealed a secret.
JUNE SMITH: She said, “Your mother was a white woman.” And I said, “A white woman?” Which was totally shocking to me.
NARRATOR: Her biological mother’s name was Ann D’Amico. June has never learned the identity of her father. When June takes her test with AncestryDNA, she checks the box asking to be linked to any customers with whom she shares DNA
Though she knows Ann has died, there’s someone else she desperately wants to find. While digging into Ann’s life story, June learned that she’d given birth to another biracial daughter, who had a different father, a girl, named Joan Moser, June’s older half-sister.
JUNE SMITH: I set out to search for her. And I would go on websites, I would do all kind of people searches looking for Joan Moser. But we could never come up with her.
NARRATOR: One day, June receives a message on her Ancestry page, telling her she has a new match with a close relative, a woman named Sigrid Gilchrist. She’d also grown up in Philadelphia, as the only child of a Black couple active in the civil rights movement. But at 16, Sigrid learned a long-hidden truth from her mother.
SIGRID GILCHRIST JOHNSON (AncestryDNA Customer): She told me I was adopted, that my mother was Italian and my father was Black. It was crushing. I had no idea.
NARRATOR: In the years that followed, Sigrid never connected with any of her biological relatives, until, by pure chance, right around the time that June tests with Ancestry, Sigrid does, too.
Ancestry reports that the two women, who share 1,641 centimorgans, may be first cousins. But June can’t help wondering: might Sigrid be someone even closer?
The two women agree to talk on the phone.
SIGRID JOHNSON: She said, “I have three questions to ask you.” I said, “Okay.”
JUNE SMITH: I said, “Were you adopted?” She said, “I was.” I said, “Are you biracial?” She said, “I am.” I said, “Would your birth mother’s name happen to be Ann D’Amico?”
SIGRID JOHNSON: I said, “Yes, she, that was her name, my biological mother.” She said, “Are you Joan Moser?” And then I said, “That was the name on my birth certificate.”
JUNE SMITH: I said, “Oh, my god, you’re my sister. You’re not my cousin.” We cried, and I just couldn’t believe it. I was on the phone with my oldest sister. Yes.
SIGRID JOHNSON: It was just like we’ve known each other forever, one-on-one spirit feeling that you can’t describe.
JUNE SMITH: Finding my sister gave me a sense of belonging. It gave me a sense of saying, “Hey, you know, we got the same blood.”
SIGRID JOHNSON: ...but I do see…
JUNE SMITH: …looks like me…
SIGRID JOHNSON: Yes.
JUNE SMITH: Look at the chin.
SIGRID JOHNSON: Yeah.
JUNE SMITH: It’s good having an older sister.
SIGRID JOHNSON: I don’t like being older, but it’s okay. I love having a younger sister.
JUNE SMITH: She understands.
SIGRID JOHNSON: Yeah, yeah.
NARRATOR: People like Sigrid and June can be connected by the D.T.C.s thanks to an amazing recent discovery about DNA We’ve known for a long time that the DNA molecule, which we carry in almost every cell in our body, contains the code that directs our lives.
The code is carried in chemical building blocks called bases. Known as A, C, G and T, they form pairs to create the familiar ladder-like structure of DNA It takes a whopping three-billion of those base pairs to make up our complete genome.
But since 2003, when scientists first read through all of those base pairs, they’ve discovered a surprising fact about more than 99 percent of them.
ELLEN GREYTAK: So, if you look at any two people, the vast, vast majority of their DNA is exactly the same, because all of the things that keep you alive, I mean, all of that has to be the same. It can’t change, otherwise it doesn’t work.
NARRATOR: But there are places in our DNA that do vary. Some of them are called “single nucleotide polymorphisms,” or SNPs. They’re spots where most of us have one kind of base pair, but some of us have another. So, instead of trying to identify all three-billion of a customer’s base pairs, the D.T.C.s do something that’s cheaper and faster. They only check out a customer’s SNPs, usually about 700,000 of them. And comparing people’s SNPs is an efficient way to see if they’re related, because when their SNPs match up, all the DNA in between the SNPs is usually identical, too.
And matching DNA segments are the telltale signs of a family relationship.
DEBORAH BOLNICK (Anthropological Geneticist): By looking at the amount of shared DNA, direct-to-consumer tests can give a quite accurate picture of relationships between individuals.
NARRATOR: FamilyTreeDNA, in Houston, is one of the four biggest D.T.C.s. Like many of them, the lynchpin of its operation is its technology for reading SNPs. And this is it, a small piece of glass called a SNP chip. It contains hundreds of thousands of tiny beads; each one holds a short piece of DNA called a probe.
CONNIE BORMANS (Laboratory Director, FamilyTreeDNA): And we put an individual’s DNA on the chip, and the part of an individual’s DNA that matches the little probe, they will bind together.
NARRATOR: Once bound, the identity of the SNP is revealed by a fluorescent dye.
CONNIE BORMANS: For example, if you have an A, you’ll see green. If you have a G, you’ll see red.
NARRATOR: The SNP data enables the lab to see how much DNA is shared by customers who’ve opted for family matching. The company website shows them their list of matches.
CONNIE BORMANS: It will show everyone that you’re related to, and the estimated relationship.
NARRATOR: But sometimes, that match list can reveal a painful truth.
CONNIE BORMANS: This anonymity and taking these secrets to the grave, with the advent of DNA testing, it really doesn’t exist anymore.
NARRATOR: That’s what Dani Shapiro was shocked to discover. A novelist and memoirist, she’s written about growing up in an Orthodox Jewish family in New Jersey, and about her parents, Irene and Paul.
DANI SHAPIRO: I was very, very bonded with my dad, much more so than with my mom. He worked on the floor of the New York Stock Exchange. And I would meet him for lunch sometimes, and he would come out, and he would just, like, fling his arms open, just like, “Hiya darling.” Give me this huge hug. It’s going to make me cry. I loved my father.
NARRATOR: From childhood on, this Jewish daughter draws comments.
DANI SHAPIRO: “You don’t look Jewish.” “You can’t possibly be Jewish.” “There’s no way you’re Jewish.” “Did your mother have an affair with the Swedish milkman?” “Shapiro your married name?” I could go on.
NARRATOR: One day, in 2016, her husband, Michael Maren, decides to take a DNA test from Ancestry. Without thinking about it much, Dani decides to take one too. She knows that both of her parents are of Ashkenazi, or Eastern European Jewish descent.
Several weeks later they get their results.
DANI SHAPIRO: We opened them, and he’s like, “Huh. According to this, you’re about 50-50, Eastern European Ashkenazi and the rest is all Western European: French, Irish, English, Swedish, German.” My only response was, “Oh, well, they must’ve made a mistake.”
It was only a few days later, and my husband came in, and he said, “You have a first cousin on your Ancestry.com page, a first cousin who we don’t know.” We don’t, we don’t know this first cousin.
NARRATOR: In search of clues, Dani turns to someone she’s sure is a blood relative.
DANI SHAPIRO: I have a much older half-sister from a first marriage of my dad’s. I recalled that a number of years ago she had done, I think, 23andMe®. And I sent her an email, and I said, “Do you have your results from, from the DNA test you did?” And she did, and she sent them to me.
NARRATOR: Dani gives the half-sister’s file to her husband. Using GEDmatch, he checks to see how much DNA she and Dani share, and discovers the truth.
DANI SHAPIRO: He said, “You’re not sisters.” And I said, “Not, not half-sisters.” ‘Cause that’s what we were. And he said, “No kind of sisters. You’re not related.”
And so, that was the moment for me when all of the pieces began to just click into place, where I thought, “Well, if he’s not one of our fathers, he’s not my father.” Something very, very important was kept from me. And it felt to me like my identity was in pieces.
NARRATOR: Her parents are both deceased. But she remembers her mother once saying she had a hard time getting pregnant, and mentioning a fertility clinic in Philadelphia. Dani and her husband track down the first cousin who popped up on Ancestry. His uncle turns out to be Dani’s biological father, a retired doctor. He’d gone to medical school in Philadelphia and had been a sperm donor at the clinic.
She searches the internet and sees a video of him giving a talk.
DANI SHAPIRO: I knew what I was seeing. And I remember getting up and walking into the bathroom and looking at my face in the mirror for the first time after seeing him and understanding my face for the first time in my life.
NARRATOR: Dani feels compelled to write a new book about family, identity and her own experience. Its title: Inheritance.
DANI SHAPIRO: My book is dedicated to my father. And sometimes someone will say to me, which father? And I’m like, “Are you kidding?” My mother wanted to bear a child. And I think it must really not have been easy for my father to have gotten to this place where he was willing to, genetically, replace himself. That’s what that is. It’s saying, “One of us is going to be the biological parent of this child and one of us is not. And no one’s ever going to know except for us.”
NARRATOR: Dani is far from alone. According to one estimate, some one-million people have discovered from consumer DNA tests that the man who raised them is not their biological father, or that they have a half-sibling they never knew about.
And there are even darker secrets that sometimes come to light. In Washington State, in 2018, the secret that Chelsea Rustad’s DNA helps to reveal could be the key to cracking a 31-year-old cold case.
CHELSEA RUSTAD: It’s really upsetting, very distressing to think about. Only a monster could do such things to people.
NARRATOR: On November 18th, 1987, two young Canadians—Jay Cook, 20 years old, and his girlfriend, Tanya van Cuylenborg, 18—leave their hometown, a suburb of Victoria, British Columbia, heading to Seattle, to run an errand for Jay’s dad.
Six days later, Tanya’s partially clothed body is found by the side of this road in Skagit County, Washington. She’s been shot in the head, and there’s evidence of rape. Two days after that, some 65 miles away, in Snohomish County, beneath this bridge, hunters find Jay’s body. He’s been strangled with twine and dog collars, his head beaten with rocks.
JAMES SCHARF (Detective, Snohomish County, Washington): We had two young, totally innocent kids that got kidnapped and brutally murdered.
NARRATOR: During the investigation, police recover potentially precious evidence from Tanya’s body: the assailant’s DNA They will run it through a lab procedure that is still the gold standard for proving identity with DNA It zeroes in on just twenty or so places in the genome where a short string of letters, for example G, A, T, A, just keeps on repeating.
They’re called “short tandem repeats,” or S.T.R.s. And scientists can count the number of times they repeat.
STEVEN ARMENTROUT (Chief Executive Officer, Parabon NanoLabs): And those counts vary, person to person, just like the ridge lines on a fingerprint. It’s a very powerful technique, because, with enough locations, you can do an identity match with very high probability, because of these slight differences one person to the next.
NARRATOR: But like a crime scene fingerprint, a crime scene S.T.R. profile is only useful if it matches one that’s already in the possession of law enforcement.
For decades, the profile in this case doesn’t match anyone known to the police. The case goes cold, until the day when Chelsea Rustad uploads a DNA file to GEDmatch, where it becomes a clue that will eventually lead the police to a major break in the case.
Chelsea’s experience will make headlines, but most DNA test takers just want to know, “What are my roots?” A seemingly simple question that often leads to its own set of mysteries.
BESSIE LAWTON (West Chester University): Don’t open anything until we ask you to. We’re going to do this one by one…
NARRATOR: These 14 people are about to experience DNA ancestry testing for themselves.
CHERRY RICHARDSON (Research Participant): ’Cause there are so many kids I’m growing up with who are all in the same situation. We don’t know our heritage. We could probably safely assume that our ancestors’ ancestors had something to do with, like, slavery and things like that, but we don’t really know where we came from.
NARRATOR: Cherry Richardson is taking part in a research study, at West Chester University, in Pennsylvania.
BESSIE LAWTON: So, we have a research protocol by which we collect data for this particular project.
NARRATOR: The study is run by two communications professors, Bessie Lawton and Anita Foeman. The question they’re asking is, “How does DNA testing affect our understanding of who we are, and also, our ability to understand what makes us different?”
BESSIE LAWTON: And after we receive the results, we bring you together.
ANITA FOEMAN: The whole idea is to listen to each other and talk with one another.
NARRATOR: Anita was inspired to start the project because of her experiences as a diversity trainer.
ANITA FOEMAN: I thought looking at our DNA was a really interesting way to approach this whole conversation about race and diversity, in a way that was not going to make people defensive. And that has happened.
TYQUINE GOLDEN: We don’t identify ourselves with Africa. We just say we’re Black. You know, we literally separated from that which we came from.
NARRATOR: In a previous test with Ancestry, Tyquine Golden was told his roots were 80 percent West African, and 20 percent British. In today’s test with FamilyTreeDNA he hopes to learn more.
TYQUINE GOLDEN: They got everybody. My suspicions might lead me to say, somewhere in slavery, 20 percent might’ve came in and have been integrated with our DNA And that might not have been voluntary.
TSHAKA CUNNINGHAM (Molecular Biologist): I think, as an African American, it’s a tough thing to grapple with, when you think about the origin of your Caucasian, or white ancestry. That often happened due to rape and mistreatment, but it is part of your history. So you have to confront it on some level and understand it. It’s part of how you got here.
TYQUINE GOLDEN: I don’t want to hide from the truth, no matter how bad it could be.
NARRATOR: Now it’s time to collect DNA…
BESSIE LAWTON: You can turn it around a little bit, to capture more.
NARRATOR: …and ship the samples off to Houston.
So, how do D.T.C.s like FamilyTreeDNA come up with a breakdown of your ancestry? It’s a process that also centers around SNPs, those places in our DNA that most frequently vary between people.
The company compares your SNPs with those of people in what are called “reference groups,” people alive today whose DNA has been tested and who share patterns of SNPs that scientists have found to be typical for the region in which they live. Those patterns are compiled into a database.
But how well does it represent test takers?
ANITA FOEMAN: They’re telling you, “This is your background, based on our database.” Well, if something’s not in their database, they can’t tell you that it’s in your background.
NARRATOR: The D.T.C.s have less data about people of African and Asian descent than they do about people of European descent.
FATIMAH JACKSON (Biologist, Howard University): Most of the genetic testing that has been done, has been done on North Atlantic Europeans. So, our reference databases are biased.
ANITA FOEMAN: Why don’t we all just take a minute and open your results, and take a look at the map for the first time.
NARRATOR: FamilyTreeDNA has given Nick Pasvanis, whose parents trace their ancestors to Greece, Germany, England and Scotland, a detailed breakdown.
NICHOLAS PASVANIS (Research Participant): I’m 45 percent Southeastern European, which is about what I expected. I’ve always felt like I was just a general European mutt, and that’s pretty much what the map shows.
CHERRY RICHARDSON: So, I was wondering, when I got it, like, if it would say if I was Black. And I am 94 percent West African, so, yeah, I’m pretty Black.
NARRATOR: But Cherry Richardson’s African bubble provides little detail.
Hana Wiessmann and Viola Wang, who were both born in China, have even bigger bubbles.
HANA WIESSMANN (Research Participant): I mean, I have just these giant bubbles, and they’re like, “You’re super Asian.” Like, I kind of already knew that, so…
VIOLA WANG (Research Participant): Basically, people who have huge bubbles are considered the minorities.
FATIMAH JACKSON: And it’s unfortunate, because it perpetuates a kind of Eurocentrism that has tainted our scholarship, that is a foundation for notions, false notions of white supremacy. And it highlights the disparities that are currently prevalent throughout science and particularly in genetics.
PAULINE SCHMIDT (Research Participant): There’s also 23 percent southeast with Italy and Greece highlighted, which was never on our radar.
NARRATOR: But there’s another problem with the way D.T.C.s calculate ancestry.
The DNA of people who lived in a place long ago, your ancestors, may be different from the DNA of the people in the reference groups who live there today. That’s because, for centuries, people and their DNA have been moving around the globe.
FATIMAH JACKSON: You really have to get over the hurdle of static thinking about human populations, that there are Irish genes and Italian genes and Nigerian genes and Zimbabwean genes. And that’s just not the way that human evolution works. Because static feeds into the racist paradigm, feeds into the me-versus-you, you know, us-versus-them.
NARRATOR: And yet it is true that certain SNP patterns are more prevalent in some places than others.
TSHAKA CUNNINGHAM: There are several clues that can link you back to areas and specific regions where your ancestors evolved. The companies are doing the best they can with the data that they have.
BENNETT GREENSPAN (Chief Executive Officer, FamilyTreeDNA): And that’s why all the DNA testing companies are trying to add more discrete populations to their database, so that when they don’t assign your population perfectly, they’re as close as they possibly can be.
NARRATOR: Bessie and Anita are finding that, whatever their flaws, DNA ancestry tests, by making people think about their roots, can help them to better appreciate human diversity.
JOAO BARRETO (Research Participant): ...the north of Africa, Middle East, the western Europe, but I was…
BESSIE LAWTON: It makes people think of their stories in relation to other people in the whole story of human migration. Most people have felt this to be a positive experience.
NARRATOR: Tyquine Golden’s results from FamilyTreeDNA are very close to those he received from Ancestry.
TYQUINE GOLDEN: Can’t ignore it now, the whole, like, Ireland and U.K. part of the DNA
ANITA FOEMAN: Let me ask, do you think you’re as authentically Black as she is?
TYQUINE GOLDEN: I don’t think it makes a difference.
ANITA FOEMAN: They sat there and had a conversation about race that was fun and exciting and joining. And if that can happen more and more, what are the possibilities?
NARRATOR: But as difficult as determining ancestry may be, the toughest challenge the D.T.C.s are taking on may be assessing our genetic disease risks, because when it comes to the accuracy of those tests, the stakes couldn’t be higher.
We all face the risk of developing life threatening diseases, but some of us face a greater risk because of variations in our genes. Deviations from the precise sequence of As, Cs, Gs and Ts that form the genetic code for making proteins: the critical molecules that keep our bodies working.
ROBERT GREEN, M.D. (Brigham and Women’s Hospital): It is hard to believe that a single letter change could affect a human being so profoundly, among this huge string of three-billion letters. But then you get those critical places where, if you’ve made that specific change, the protein simply doesn’t work anymore.
NARRATOR: Several of the D.T.C.s now offer testing for genetic health risks. But how reliable are they?
Most of those tests look only at selected SNPs and ignore the rest of the genome, where other risks may be lurking, risks that they will inevitably miss. One example: 23andMe’s controversial test for breast cancer risk. It looks at two genes called BRCA, or “braka” genes. They code for proteins that control cell growth.
But certain base pair variations derail the BRCA genes and make some cancers, such as pancreatic, prostate and especially ovarian and breast cancer, more likely.
Scientists have documented close to 4,000 such variations; 23andMe sells a SNP test that looks for three of them.
They’re among the variations that put women at very high risk for breast cancer. Each can be reliably detected by SNP testing. And each is 10 times more common in women who have Ashkenazi Jewish ancestry.
Jessica Algazi, a 52-year-old entertainment lawyer in Los Angeles, has three Ashkenazi grandparents. In 2018, she takes the 23andMe BRCA test, having no idea it will change her life. One day, when she’s playing golf, she gets an email.
JESSICA ALGAZI: I get the results as I’m sitting on a golf course in a golf cart and I looked down and, like, “Oh, my god, I can’t believe this.”
NARRATOR: 23andMe reports that she has a BRCA1 variation that makes it highly likely she will develop ovarian or breast cancer. A second test, by a DNA lab that specializes in BRCA testing confirms it. Although she is cancer free for now, she makes a decision.
JESSICA ALGAZI: My gynecologist said, you know, “Jess, you got to do something now. You’ll have your ovaries and tubes removed, and you need to have a double mastectomy right away.” And so, I’m just grateful that I was able to find out in time to do something, before I got sick. I’m eternally grateful to the folks at 23andMe for giving me that opportunity. They, quite possibly, saved my life.
NARRATOR: But most women who have BRCA variations don’t have any of the three that 23andMe tests for, women like Pamela Munster. She happens to be an oncologist, in San Francisco, who specializes in breast cancer.
PAMELA MUNSTER, M.D. (University of California, San Francisco): I have the BRCA1 gene.
NARRATOR: She has no Ashkenazi Jewish ancestry. In 2010, Pamela takes 23andMe’s BRCA test herself.
PAMELA MUNSTER: What I learned is that I didn’t have much of a breast cancer risk, and by 23andMe’s reckon, my breast cancer risk was actually quite low.
NARRATOR: But, in 2012, Pamela is diagnosed with breast cancer.
PAMELA MUNSTER: And the way that my cancer looked under the microscope, I had the sense that this breast cancer was associated with a BRCA mutation.
NARRATOR: To confirm her hunch, Pamela has her DNA tested by what’s known as a clinical lab, the kind doctors use. They don’t just look at scattered SNPs. They look at every single base pair in genes, a process known as “sequencing.”
PAMELA MUNSTER: They go through the entire BRCA gene. And they, remember, these are like 80,000 base pairs, and they can tell you is the letter there? Is the letter not there?
NARRATOR: Pamela turns out to be right. She does have a BRCA2 mutation. But it’s not any of the three variants 23andMe tests for. It’s one of the thousands of others.
PAMELA MUNSTER: If I just want to know who I’m related to, 23andMe, Ancestry are very good tests. If you want to know, do you carry a BRCA gene and are you at risk for breast cancer? I think 23andMe is not an ideal test.
NARRATOR: But 23andMe says that its BRCA test has alerted some 3,000 people to their cancer risk. And that choosing these three variants makes sense, because they confer such high risks.
SHIRLEY WU (Director, Health Product Science, 23andMe): What these variations mean for someone’s risks is very, very well understood. The studies that have shown near, nearly half of people carrying one of these variants don’t realize it.
ROBERT GREEN: So, it’s great for those people who were not even thinking they were carrying that mutation to pick it up with direct-to-consumer testing. It’s not a good thing if those people think they have been exhaustively tested, because they have not.
NARRATOR: And there are also concerns about how test takers’ data is used.
In 2018, 23andMe agrees to share anonymized information about millions of its customers with GlaxoSmithKline to use in the development of new drugs.
23andMe says some 80 percent of its customers have given consent for their data to be used in research. Most have also filled in health questionnaires, enabling valuable links to be made between their genes and their health histories.
SHIRLEY WU: The potential of what you can do with that information is just astounding.
NARRATOR: But while the possible rewards of the deal seem clear, to some it raises ethical questions.
ALONDRA NELSON (Sociologist): You’re actually paying your money to give your data to a company. And then it will be capitalized on, potentially, without benefit to you. When you’re dealing with such a new technology, I think the full implications can’t possibly be understood by consumers because things are just too new.
NARRATOR: So, how safe is the data of 23andMe’s 12-million customers?
JACQUIE HAGGARTY (Privacy Officer, 23andMe): We do not sell data.
We do not share your data with any insurance company or any employer, hard-stop, without your consent.
NARRATOR: Federal law prohibits most employers from using genetic data to make workplace decisions and prohibits health insurers from using it to change or deny coverage. But disability and life insurance companies are free to use it.
While 23andMe and FamilyTreeDNA talked with NOVA about these issues, AncestryDNA declined to participate in this film.
The risks inherent in new technologies often become obvious only in hindsight. Chelsea Rustad could never had predicted that her DNA test might lead the police to a dangerous murder suspect. They found him, using a new investigative technique that springs directly from the rise of consumer testing.
It’s called genetic genealogy. And before it was used to solve crimes, it was used by people looking for their birth parents. One of its pioneers is a retired patent lawyer named Barbara Rae-Venter.
BARBARA RAE-VENTER (Genealogist): I really backed into this whole thing, because I was doing unknown parentage type work with adoptees. For adoptees, DNA has been huge, because for them to try and figure out who their birth relatives were just using paper. It’s very, very difficult.
NARRATOR: Barbara starts by connecting the adoptee to the people on their DNA match list. Then, by digging through records she finds more relatives. The goal: find an ancestor who links everyone together and points directly to the birth parent.
In 2017, Barbara is asked by investigators in California to try to solve a different kind of mystery: one of the nation’s most notorious cold cases.
The so-called “Golden State Killer” was suspected of committing at least 13 murders and more than 50 rapes during the 1970s and 80s. Police have long had his DNA, but they have no idea who he is. Barbara agrees to help.
From the crime scene DNA, a SNP profile is made, and then uploaded to GEDmatch. Using the relatives who pop up, Barbara creates a family tree and eventually zeroes in on a man named Joseph DeAngelo. A one-time policeman, DeAngelo had never been under suspicion. Police collect his DNA and run an S.T.R. test. The result? A perfect match with the DNA of the “Golden State Killer.”
JUDGE: Murder in the first degree, that charge, sir, how do you plead?
NARRATOR: In June, 2020, Joseph DeAngelo pleads guilty to 13 counts of murder.
JOSEPH DEANGELO: Guilty.
NARRATOR: He is sentenced to life in prison.
At the time of DeAngelo’s arrest, Detective Jim Scharf is amazed to learn what’s been accomplished using genetic genealogy. He quickly thinks about Tanya and Jay.
He reaches out to a computer scientist he’s been working with in Virginia, Steve Armentrout.
PAULA GAWTHORP-ARMENTROUT (Parabon NanoLabs): So, do I need to hardwire the number in here, or am I doing a calculation?
NARRATOR: Steve’s company, Parabon NanoLabs, has developed methods and software for sifting through hundreds of thousands of SNPs.
STEVE ARMENTROUT: We first have to get DNA from the crime scene into a format that can be used for uploading. Jim gave us the okay on a Thursday; on Friday, we were uploading to GEDmatch.
NARRATOR: Steve has teamed up with a genetic genealogist in California, CeCe Moore.
CECE MOORE: On Saturday morning, I rolled out of bed, before I even put my contacts in and flipped open my laptop to see if we had that match list. And we did.
NARRATOR: GEDmatch shows two people who each share around three percent with the unknown suspect.
CECE MOORE: So, to have two people that shared about three percent of their DNA, or enough to be a second cousin with the suspect, did feel like getting struck by lightning. Second cousins will share a set of great-grandparents, and that’s not that far back in the tree. In genealogy, I can almost always get back to someone’s great-grandparents.
NARRATOR: One of Cece’s two top matches is Chelsea Rustad. The other is a cousin who’s never been publicly identified. They both share DNA with the suspect but don’t share any with each other.
CECE MOORE: That meant that they represented different branches of the suspect’s family tree. I really lucked out. I found an obituary from a woman who was carrying the surname that I had just seen in the other match’s family tree. So, that told me we have a woman from this tree and a man from this tree who have married, and, hopefully, had children.
NARRATOR: CeCe knows that if they did, those children would carry a mix of DNA very similar to that of the suspect.
The couple had four children.
CECE MOORE: We got really lucky that there was only one male in this family, because the genetic genealogy was pointing at one person and only one person, and that was William Earl Talbott, II.
NARRATOR: At the time of the murders, Talbott lived a few miles from the bridge where Jay Cook’s body was found. Now, he is 55, a truck driver. The police follow him. They want his DNA to see if it matches the DNA from the crime scene.
One day they get lucky. A drinking cup falls out of his truck.
Jim Scharf brings the cup to the Washington State Patrol Crime Lab for S.T.R. testing. Lab supervisor Lisa Collins asks him to wait. Soon, she returns.
JIM SCHARF: Lisa turned and handed me the report and said, “Jim, it’s him. There’s a match.” And I couldn’t believe it.
My eyes teared up. I yelled out a scream. “This is wonderful. We finally got this guy.”
NARRATOR: On May 17, 2018, William Earl Talbott, II is arrested on a charge of first degree murder for a 31-year-old crime. He’s a man who was identified, not because he took a DNA test, but because a relative did. Someone he’d never even met.
In June, 2019, the jury delivers its verdict.
CAPTION: We the jury, find the defendant, William Earl Talbott, II, guilty of the crime of first-degree murder, as charged in count one.
FOREPERSON: We, the jury, find the defendant, William Earl Talbott, II, guilty of the crime of first-degree murder, as charged in count one.
NARRATOR: Talbott is the first suspect identified by genetic genealogy ever to be convicted by a jury. He is soon sentenced to two consecutive life terms in prison.
CHELSEA RUSTAD: It has been reiterated to me so many times by the investigators, that they wouldn’t have come this far without my DNA It would have been dead in the water.
NARRATOR: Since Talbott’s conviction, the Parabon team has used genetic genealogy to identify more than a hundred criminal suspects. But just being named by a genealogist isn’t enough to get a person arrested.
JIM SCHARF: We have to get confirmation DNA using S.T.R. testing, before we have probable cause to make an arrest.
NARRATOR: Even so, to critics, the use of genetic genealogy by law enforcement raises privacy questions.
ALONDRA NELSON: Do we want to catch people who have committed heinous crimes? Absolutely, yes. But what DNA profiles are being trolled through? What failed attempts to find suspects are we not hearing about and the data violations and privacy violations that happen along the way?
NARRATOR: The genetic genealogy team at Parabon says the fears are exaggerated.
ELLEN GREYTAK: People have control over whether their DNA is used in these investigations. Simply taking a DNA test at 23andMe, at Ancestry, your DNA is in their private database.
NARRATOR: But there’s little regulation, and policies vary. In 2019, FamilyTreeDNA apologized for letting the FBI search its database for people who share DNA with crime scene samples without customers’ permission. FamilyTreeDNA and GEDmatch both now say they only do so with explicit permission. And another worry: consumer DNA companies, like any that collect data, are vulnerable to hackers.
Yet the risks are clearly not deterring everyone.
BENNETT GREENSPAN: No one is forcing anyone to take a DNA test. If your paranoia and fear of big brother is greater than your interest in reading the medical and history book written into your cells, then I think that you should not test.
TYQUINE GOLDEN: There’s beauty in, you know, understanding where you’re from, and then searching for that.
NARRATOR: The consumer DNA phenomenon is changing many people’s lives by revealing the secrets that lie hidden deep inside ourselves. But are its benefits worth its costs and risks?
PAMELA MUNSTER: Do I want to know that I’m at risk for Alzheimer’s when there’s absolutely nothing I can do about it? Maybe not.
DANI SHAPIRO: With these DNA tests as popular as they are, the chances are that everyone who has had a secret of this nature kept from them is going to find out. Our hearts and our minds don’t know fully how to grapple with what we’re being asked to grapple with.
BESSIE LAWTON: I think the surge in DNA testing over the last 20 years has opened people’s minds to the possibility that they share more with other people than what they thought they did.
TASHAKA CUNNINGHAM: That one percent that makes us different is really just the beautiful diversity in the natural world. And it’s not that one genotype or genome is better than another, it’s just, they’re beautifully different.
FATIMAH JACKSON: The more we are tested, the more we see how connected we are to each other. And perhaps, if we see that we’re connected to each other, we’ll treat each other a little bit better.
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This program was produced by WGBH, which is solely responsible for its content. Some funders of NOVA also fund basic science research. Experts featured in this film may have received support from funders of this program.
Original funding for this program was provided by the Alfred P. Sloan Foundation, Draper, the David H. Koch Fund for Science, the NOVA Science Trust, and the Corporation for Public Broadcasting.
Image credit: (Anthropological geneticist, Deborah Bolnick)
© WGBH Educational Foundation
- Jessica Algazi, Steven Armentrout, Deborah Bolnick, Connie Bormans, Lisa Collins, Tshaka Cunningham, Anita Foeman, Sigrid Gilchrist Johnson, Tyquine Golden, Robert Green, Bennett Greenspan, Ellen Greytak, Jacquie Haggarty, Fatimah Jackson, Bessie Lawton, Cece Moore, Pamela Munster, Alondra Nelson, Nick Pasvanis, Barbara Rae-Venter, Cherry Richardson, Chelsea Rustad, James Scharf, Dani Shapiro, June Smith, Viola Wang, Hana Wiesmann, Shirly Wu