To prepare to take a cheek swab sample, you also have to refrain from eating for about an hour before. Swab kits generally contain more components, including one or two swabs and containers to protect the used swabs from contamination. We found it easiest to organize all the pieces first, to prevent any fumbling with a sample collection swab in hand. Some cheek cell kits put a stabilizing liquid in the sample containers, which required extra caution to prevent spilling.
If you have the Health + Ancestry Service you have access to the full 23andMe experience. If you only have the Ancestry Service, you can easily upgrade to the Health + Ancestry Service for £90 which gives you access to all 125+ reports on ancestry, traits and health. You are eligible to upgrade once you have received your Ancestry reports. To upgrade, log in to your 23andMe account and navigate to the Settings page. You will receive immediate access to your new health reports.
In McCartney’s view, enough testing is already done in this country (sometimes too much) and there are issues of regulation and “informed consent”. “People are given very dramatic reasons to have these tests – it could help save your life, it could help improve the quality of your life – but where is the actual controlled evidence that these tests have ever done that? There’s no evidence that says doing these tests makes people become healthier.”
DNA Clinics will always advise an appointment for your DNA test. However, there are occasions and circumstances when our customers prefer to collect their own mouth swab samples for DNA testing. DNA Clinics self-collection DNA testing kits are available to order by telephone by calling 0800 988 7107 or on-line at www.homednapaternitytest.co.uk. DNA test kits ordered on-line are sent out for FREE. The payment for your chosen DNA test is payable when you return your samples to DNA Clinics.
As it happens, most of the data on 23andMe seems harmless and fun. There are the “Neanderthal variants” (I have fewer of them than 58% of 23andMe customers, thank you very much), the bizarre earwax/earlobes-type data and, apparently, I have the muscle composition generally found in “elite athletes” (fancy). On the downside, my lineage isn’t as exotic as I’d hoped: 99.1% north-western Europe, of which 71% is British/Irish, with just 0.01% “Ashkenazi Jewish” to offset the genetic monotony. At £149, the 23andMe kit isn’t cheap and I’m quite tempted to demand a recount.
Self-collection DNA test kits are a convenient and more affordable option. However, the support and advice you receive when making an appointment to have your DNA sample taken is invaluable and we will always recommend this option to you. To locate your nearest DNA testing clinic, pharmacy or mobile sample collection service please use the location search tool.
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.
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.
When asked about how database size affects ancestry results, David Nicholson, co-founder of Living DNA, told us, “The tests absolutely rely on the reference database. If you have Polish ancestry but there are no people in the database who are Polish, then what the test will do is show what the next closest group is next to Polish, like German or Eastern European ancestry.” Each ancestry DNA service has its own sample database and reference panel made of the DNA samples collected from their users and information collected from sources like the 1000 Genomes Project. The database consists of all this information collectively. A reference panel is made of certain curated samples with known family history and roots in a specific place. The services use insights gleaned from the reference panel to give you geographical ancestry results. In theory, a larger database leads to more information available to create a good reference panel, which then leads to better results for customers.
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.
The spit is for one of the home genetic-testing kits I’m sampling. A growing number of these kits (brands such as 23andMe, DNAFit, Thriva, MyHeritage DNA, and Orig3n) promise to unlock the mystery of your genomes, variously explaining everything from ancestry, residual Neanderthal variants, “bioinformatics” for fitness, weight loss and skincare, to more random genetic predispositions, denoting, say, the dimensions of your earlobes or the consistency of your earwax.