Alternatively, if you believe your "Italy/Greece" result indicated your known Italian heritage, it is possible that your son simply did not inherit the associated DNA from you. We all inherit roughly half our DNA from each parent, but the DNA we inherit is selected at random, and so even full siblings can have different ancestry results, depending on which genetic variants they inherited.
Whether it’s an autosomal test, a Y-DNA test or an mtDNA test, virtually all providers use the same science. Some providers offer an ‘off the peg’ solution such as Ancestral Origins™ or AncestrybyDNA™, so if you’re interested in these you should shop around for the lowest price. Most providers offer a test that interprets and presents the results in a unique way, so if one of these catches your eye, look for examples of how the results are presented on their website before you buy.
Because it is a genetic condition, FH is present at birth, meaning most people with this condition have high LDL cholesterol levels from a young age. Since many people with FH show no physical symptoms, this condition is typically diagnosed with a blood test for cholesterol. However, some people with FH may not be diagnosed until after experiencing symptoms related to early heart disease, including chest pain or heart attack.
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”.
There is one really, really important thing to know about this estimate, however.  Each child inherits 50% of their DNA from each parent.  That means that 50% of their parents’ DNA does NOT get passed down to the child.  This can mean that a child of a 100% Eastern European person will only show 50% Eastern European DNA, and their grandchild will only show 25%, and their great-grandchild 12.5% – in a perfect scenario.

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?
Specific tests for your father’s family include ‘Y-DNA’ tests which focus on the ‘Y chromosomes’ in your cells’ nuclei, passed down from father to son. Specific tests for your mother’s family include ‘mtDNA’ tests which report on a subset of DNA found in the ‘mitochondria’ (your cells’ energy factories), passed down from mother to son or to daughter.
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.
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.
Y-DNA Tests: Y-DNA testing examines the Y chromosome passed only from father to son and can therefore be used to gain a better understanding of your paternal line. This can be a very interesting study for those focused on surname research, especially since the Y chromosome can give information about deep and recent roots. Because only men carry this chromosome women will need to test their father, brother or other male relation to use this test for genealogy purposes. Again, FTDNA is the leader in this type of testing and has a wealth of information, groups and forums to help.