For our evaluations, we assembled a group of testers willing to spit into a tube on camera. We chose four individuals of varying backgrounds. Two had previously taken one or more DNA ancestry tests, and two had not. Two had fairly well-documented family histories to compare against, one was adopted, and one had information about one side of the family, but not the other. All of us took DNA tests from AncestryDNA, 23andMe, National Geographic and Family Tree DNA. One tester also took each of the five additional tests we reviewed. After collecting spit and cheek cells, we mailed all of the tests at the same time and waited for results, noting all communications from the company in the meantime and how long it took each service to notify us that results were ready to view. We collected data based on testers’ impressions of their results, each service’s features and extras, how easy it was to use and navigate the service’s website, along with several other factors. We added this testing data to rigorous research and information gleaned from conversations with representatives from Ancestry, 23andMe, MyHeritageDNA, LivingDNA, Humancode (now owned by Helix) and 24genetics. 
You control your account privacy. Findmypast and Living DNA keep your data private unless you choose to share information, such as your family tree or DNA results. Your data is encrypted and stored on secure servers, only accessible by staff, vital service providers (such as our laboratory partners) and you. Living DNA has carefully chosen a European laboratory to conduct its DNA testing. Findmypast and Living DNA only disclose your data to third parties where we have appropriate agreements in place. For example, trusted third-party payment processing companies. Findmypast and Living DNA are ISO accredited for data and information security.

23andMe is an excellent DNA ancestry test because of its highly specific results and vast geographic reach – it serves more than 1,000 geographic regions worldwide. The service tests autosomal, mitochondrial and Y-DNA to give you a complete picture of your genes. Four testers took 23andMe DNA kits during testing. We received our results 32 days later, and testers were highly satisfied with the overall experience, from ease of sample collection to the thoroughness of the results. Recently, the company updated its database and increased the number of geographic regions from around 170 to more than 1,000. The updated ancestry reports are also more detailed, especially for non-European regions. 23andMe’s ancestry tests give you information split into several different reports spanning your ancestry composition, maternal and paternal haplogroups, neanderthal ancestry and DNA family. Testers particularly liked the timeline feature, which estimates when your most recent ancestor lived in each of your matched regions. While 23andMe does offer DNA relative matching and some tools to compare your genes to your DNA relatives, it doesn’t have robust genealogy tools, as its focus rests more in personal discovery and exploration. To that end, 23andMe has an optional health upgrade that provides reports on DNA traits like hair color and genetic predispositions to certain illnesses and diseases. It is the only DNA test with FDA approval for testing genes linked to conditions such as Type 2 diabetes, certain types of cancer, late-onset Alzheimer’s disease and Parkinson’s disease. If you’re interested in the health portion of the test, we recommend buying the Health + Ancestry test together, as this option costs less than upgrading later.
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.
My own results are eagerly awaited: the whole process takes about 6 weeks. I am somewhat more sceptical having Polish heritage and therefore my contact with relatives might be less likely, however I am waiting eagerly to see whether I have any trace of the Mongol hoards who invaded deep into Europe. I have posted a screenshot of how long the process takes from activation.
Although the project states that most participants won’t receive any useful information, patients will be told if something is found in their genome that is relevant to the treatment, explanation or diagnosis of their condition. They can also choose to learn if they have a genetic risk factor for another disease, such as the BRCA1 gene mutation that can cause breast cancer. Genomics England will only look for risk factors that are linked to a disease that can be treated or prevented. Untreatable conditions, such as Alzheimer’s, are not looked for.
Every company providing DNA testing has their own database of DNA samples. These are called AIM’s or ancestry informative markers. These markers were derived from the current populations of America, Asia, Europe and Africa. Every database is looking for a pair of genes located on a specific chromosome in a specific position. The way the DNA is evaluated is through the SNP’s or the single nucleotide polymorphisms. The SNP’s are chosen according to the frequency in a specific geographical population. Your SNP’s are compared to the most common SNP’s for the various populations in the company’s reference database. The results are not conclusive because they are based on common genetic variations. The probability for your DNA being from a certain country is based on a comparison between your DNA and the database. If you used a different company, they would have a different database. This means your results would most likely differ. According to studies, the lowest concordance is with individuals of South Asian, East Asian and Hispanic descent.
Bill Newman, professor of translational genomic medicine in the Manchester centre for genomic medicine at the University of Manchester, and chair of the British Society of Genetic Medicine, says that such tests in this context simply don’t make sense and that, usually, telomere testing would only be used in in-depth studies of ageing and diseases associated with ageing. “There’s some really brilliant work going on, by some of the best biologists in the world,” says Newman, citing Elizabeth Blackburn, who won the 2009 Nobel prize for medicine for her work on telomeres. “But there’s no evidence whatsoever that measuring a person’s telomeres gives any indication about their health – or beauty, intelligence, or anything else that might be listed on these sites.”
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.
Note that DNA testing isn't the only kind of kit that collects physical evidence from you these days. Ubiome is one noteworthy example. The service evaluates your microbiome—basically the bacteria that live in and on you. In our review, we took its gut biome test, which required our intrepid reviewer to send in a poop sample (insert poop emoji here).
It may cost a little more, but I would highly recommend saving the extra and using DNA Tribes® rather than spending over half the cost for minimal tribal/biogeographical pinpointed information. The primary benefit of STR rather than SNP testing is the availability of rich reference data. DNA Tribes® tests industry standard autosomal STR systems, which allow the identification of a person’s DNA profile not shared with any other person. Because these STR markers have been tested and used in the court systems around the world, they allow DNA Tribes® to perform the most thorough comparison of a person’s own DNA profile to over 1,200 ethnic groups (populations) around the world. At present, SNP testing from these other autosomnal DNA testing kits does not yet match the geographical detail of DNA Tribes® autosomal STR analysis.
Since genome sequencing is still a relatively young science, we don't recommend submitting your child’s DNA to direct-to-consumer companies. We do encourage consulting with your doctor about genetic testing for your child. Due to some concerns with the DNA testing industry, the choice to have one’s genes sequenced by a private company should be made with informed consent. Those concerns are magnified when applied to children, who cannot make their own decisions regarding the unlikely potential risks or privacy concerns.
“My concern is that more and more of these tests are being put out, and people are being persuaded to have these tests done, and they get results back that are very often of very low value and dubious helpfulness,” she says. “And often people are told to go to see their GP and that then places a direct stress on the NHS, at no cost to the company. The companies make their profits and walk away, letting the NHS sort out all the fallout, the push-back, from the test results, in a way I find absurd. Why should the NHS have to prop up the problems that these companies create?”