Hi Mark, Thank you for your article – very helpful. I am adopted from Asian country and live in Australia. I don’t know who my biological parents are and don’t know if I have any siblings. I have been researching through all these websites trying to decide which dna test to take – confused by it all. Your article has helped me to decide on FTDNA (family history and mtDNA) – hoping that it would give me ancestry makeup inherited from my bio parents and ancestry details on my mothers side (as I am female, limited to this test). In… Read more »
Thank you for such detailed information. I’m considering buying a DNA ancestry kit for my wife for Christmas (and buying one for myself as well). After reading your article (and many of the wonderful comments), I’m leaning towards the one from Ancestry.com. However, would I still get complete results without a subscription? I looked on their website and it doesn’t say.
23andMe started out by testing for genetic markers of diseases and medical conditions before rolling that back in response to the governmental concerns. It has since started slowly adding more health-related features with approval from the FDA. In April, 23andMe got approval to offer risk analysis for ten genetically linked diseases. The company now offers two options: Health + Ancestry ($199) and Ancestry ($99). The Health + Ancestry plan includes testing for genetic health risks and carrier status, as well as reports on your genetic weight, hair loss, and other traits.
When my results appear, they show nothing bad. If anything, it’s anticlimactic: cholesterol, vitamins, liver proteins and the like are all in the normal range, with only ferritin (iron stores) slightly high, with a recommendation to go easy on any iron supplements. My problem with the baseline test is that, unlike Thriva’s other products, clients are supposed to have one every three months to keep track, but would I really want (or indeed need) to do such a test so regularly?
The only patients having their genome sequenced are those with certain cancers or rare diseases. In some cases, family members may also be asked to participate. To take part, a patient must first be referred by a consultant, before being taken through an extensive consent process to ensure they know what participation in the project means. As well as the genome sequence, Genomics England asks for access to a patient’s lifetime medical records so that links can be made between their genetics and their individual disease. The NHS has made it very clear that, for many participants, taking part in this project won’t help them treat their disease. But it is hoped that the information they provide will go on to help treat others in the future.
Who knows how much of it made solid scientific sense? However, I have to confess that I rather enjoyed it on the level of an indulgent genome-oriented “pampering session”, just as I had a hoot with the ancestry/Neanderthal/earlobe data on 23andMe. Where Thriva is concerned, I also noted that it did advanced thyroid tests. Although such tests are available from the NHS, I’m hypothyroid myself and I know that sometimes it can be difficult and time-consuming getting tests repeated and it could be useful to be privately tested in this way.
If the company responsible for running your test is sold, whatever you signed loses significance due to the privacy policies of the company. Despite most of these privacy policies stating they will notify you of any changes, you would have to keep in constant contact with the company to ensure you were actually aware of these changes. The people willing to do this would be far and few between. Unfortunately, even if your name is not located within the database, this does not mean other databases cannot be used to determine your identity. In one specific case, a woman had a DNA test run. She found out she had a half-sibling. Although she was very excited about this news, this type of information would devastate numerous individuals.
Health & Wellness tests: There are a ton of health and wellness DNA tests. We found several specifically oriented to dieting and weight loss, including embodyDNA, Vitagene, DNAFit and the several options available through the Helix marketplace. While there definitely are some links between DNA and factors that contribute to weight, we advise taking these diet plans with a grain of salt, as DNA science is still a relatively young field. We similarly advise caution for the multitude of non-diet health and wellness DNA tests, which offer insights into your sleep, food sensitivities, and vitamin and mineral levels. And double that for medical information found in consumer DNA kit test results. While medical insights learned from taking an at-home DNA test may be interesting, it’s best not to take them too seriously. If you have a concern about a genetic predisposition to a disease, it’s best to talk to your doctor instead of relying on a direct-to-consumer kit.
Rather than simply looking at your DNA in isolation, the Findmypast DNA test analyses unique combinations of linked DNA. This proprietary method delivers a level of detail impossible with other ancestry DNA tests. It also uses the latest technology, which is constantly updated in response to the latest industry innovations and peer-reviewed research. As the technology evolves so too does the detail of your test results, which will receive free ongoing upgrades.
Most of this trait data tells you things you already know, like your hair and eye color, but it is fun to see them compared to your genetic relatives and the world at large. We also found it fascinating to learn more about how these physical traits are genetically determined. For example, finger length ratio is determined by hormonal exposure in the womb, with higher testosterone exposure resulting in a better chance of having a longer ring finger. 23andMe’s Health report for finger length ratio looks at 15 gene markers to estimate your likelihood of having longer ring fingers or index fingers.
The 100,000 Genomes Project is an NHS initiative, run by Genomics England, and is the largest national genome sequencing project in the world. On entering, patients have their entire genome, of more than 3bn base pairs, sequenced. This is different from commercially available genetic testing kits, such as those from 23andMe, which only look at very small stretches of DNA in a process called genotyping. The hope of the NHS is that having so much genetic information, from so many different people, will allow “groundbreaking discoveries about how diseases work, who could be susceptible to them, how we can treat them, and what treatments might work”.
Once your genetic information is out there, it’s difficult to undo. Also, once you know something about yourself, it’s impossible to un-know. Revelations such as having different parents than you expected or finding unknown half-siblings are difficult to process at any age, but it’s particularly troubling for kids. However, you can always simply opt out of family matching features.
Findmypast & Living DNA are excited about the opportunities this partnership creates for everyone from serious genealogists to those just starting to explore their family history. As we focus on the best of British and Irish family history, we are committed to continue making improvements to the Findmypast DNA test to make it possible to not only discover where your ancestors came from, but learn their amazing stories too.
Unless expressly indicated in the product description, Amazon.co.uk is not the manufacturer of the products sold on our website. While we work to ensure that product information on our website is correct, manufacturers may alter their product information. Actual product packaging and materials may contain more and/or different information than shown on our website. If you have any specific product queries, please contact the manufacturer. This notice does not affect your legal rights. For medicinal products, content on our website is not intended to be used to diagnose, treat, cure, or prevent any disease or health condition or to substitute advice given by medical practitioners, pharmacists or other licensed health care professionals. You should contact your health care provider immediately if you suspect that you have a medical problem. You should always read the labels, warnings and instructions provided with the product before using or consuming it and not solely rely on the information presented on our website.
Kits are despatched within 5-7 days of purchase date. The delivery time for your kit will vary depending on the postal service you have selected. Once you receive your kit, follow the simple instructions to activate it and send us your DNA sample. If you’re a new or returning Findmypast customer, you’ll receive a complimentary 14-day Findmypast subscription when you activate your kit.
WARNING: AncestryDNA highly discourages the purchase of our DNA kit from unauthorized resellers. To ensure the best experience and service, please purchase directly from AncestryDNA. DNA kits that are fraudulently purchased and then resold through Amazon may be deactivated by AncestryDNA, and may not be eligible for a refund. Before you can use AncestryDNA and see your results, you must create an Ancestry account and agree to Ancestry's Terms and Conditions and Privacy Statement. Actual product packaging and materials may contain more and different information than what is shown on our website. We recommend that you do not rely solely on the information presented and that you always read labels, warnings, and directions before using or consuming a product.
Finally, if you happen to meet a special someone on DNA Romance and want to see what your future child together might look like, there’s BabyGlimpse by HumanCode. Like a very advanced Punnett square, BabyGlimpse compares your and your partner’s DNA to create a profile that examines which traits your offspring might inherit, including things like ancestral DNA, eye color and lactose intolerance.
Then comes the section about serious genetic variants. So far as “counselling” goes, previously, I’d waved away concern for my psychological welfare from the Observer’s science editor (“I’m a former goth,” I said. “My default setting is ‘doomed’”), but it turns out to be quite daunting. It doesn’t help that I initially mistake the full list of potential conditions for my own results, hence (thankfully briefly) thinking that I have higher risk factors for everything going. It makes me wonder – how many other people are going to do that?
The first kit I try is Thriva’s baseline test (£49), which, like all its products, checks your blood. The box arrives promptly enough (containing spring-loaded needles, a little collection tube, antiseptic wipes, plasters, etc), but there’s a problem. The idea is to prick your finger and massage blood into the tube, but I just end up making my fingers sore and what I get out barely smears the top of the phial. Maybe it’s just me, but it turns into a right faff. In the end, I take advantage of Thriva’s service to send someone out to take a sample of blood from my arm.