Although, I have absolutely no British or Irish ancestry, I found my results extremely satisfying. I particularly appreciate that living DNA gives you a lot of ways to view your data. You can see your ancestry results as color-coded dots filling up a person’s silhouette, on a map, as a pie chart or on a timeline. All the graphics present the same set of data, but each has its own appeal. Within each graphic, you can also choose to view global or regional matches and cautious, standard or complete estimates, which each have a different level of detail and certainty.
In Newman’s view, the genie is out of the bottle with home genetic-testing kits. He says that while the kits could potentially provide data in the future, right now, they lack “clinical utility” – they look at genetic variants that, individually, have a very low chance of predicting specific health risks, as there are too many variables: “It’s like the Opportunity Knocks clap-o-meter, with some people further along the scale, and therefore more likely to get the condition and then people at the other end of the scale, who are unlikely to get it.”
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.
Familial hypercholesterolemia (FH) is a genetic condition associated with very high levels of cholesterol in the blood, specifically low-density lipoprotein (LDL), or "bad" cholesterol. High cholesterol due to FH increases the risk for early cardiovascular disease, which can lead to a heart attack. This test includes 24 genetic variants linked to FH.
Offering DNA test kits and a range of online subscription services, MyHeritage says that its database includes more ethnicities -- that's 42 -- than any other major testing service. The free 14-day trial will let you poke around the company's massive online database which includes 3.5 billion profiles in addition to information about over 100 million subscribers and their collective 46 million family trees.
the beauty of a y-DNA test is that it tracks the paternal y-chromosome…..yes, even indicating a surname change but not when the surname changed [does not match known male descendants]. In all DNA testing, it really helps to have researched about 5 generations back on all lineages……that way you can find common surnames in the autosomal tests. The y-DNA tests go back for centuries…..and the autosomal testing really only goes back about 5 generations…….
There is currently no known cure. People with AAT deficiency are encouraged to avoid smoking and consider getting certain vaccinations. For those with symptoms, treatment focuses on management of lung and liver problems. Direct replacement of the AAT protein into the blood may be used to slow the progression of lung disease. Lung and liver transplants may be beneficial in some cases.
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.
McCartney says that anxious people often contact her, saying they wished they hadn’t done the tests. “These companies often say that it’s worth it for the helpful advice. But I can give you really good advice right now without seeing a single test result: be active, have lots of social networks, do work you enjoy, try not to smoke or drink too much, don’t be overweight or underweight, eat lots of fresh fruit and vegetables. Nobody needs to get tests done to get that kind of basic lifestyle advice.”
Most ancestry DNA kits cost about $100. AncestryDNA, 23andMe’s Ancestry test and National Geographic’s Geno 2.0 test all fall nicely into that price point. If you’re looking for a bargain, we recommend waiting to buy until your preferred test is on sale, as they’re often available well below their usual price. To get the most for your money, buy an Ancestry or 23andMe kit on sale then upload your raw data to MyHeritage DNA’s database, which is free.
I can’t help you with your question Robin, but you make a good point. I have had my DNA tested (only with MyHeritage so far) and the “North and West European” part is so broad (it could be anything from France, Belgium, the Netherlands, Luxembourg, Germany etc but it would have been important to have more detail as it is really what I would have loved to know more about) and then 0.8% Middle East…
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.”
MyHeritage shows cousin matches as part of your DNA purchase for free and has some really wonderful tools to connect your research to your DNA matches. Using smart matching features to see how your tree is connected to others, and adding records you discover this way, may cost an additional monthly fee however. Still, MyHeritage is generally less expensive than Ancestry. You can also try their record collections for free here.
In the case of a great-grandchild, or a great-great-grandchild, something even stranger can happen. Remember that a child will get half of their mother’s DNA, but there is never ever guarantee which 50%. The way it is chosen is fairly random, as far as scientists know. Take the example of the 100% Eastern European person. Their great-grandchild will inherit 50% of their DNA from their part-Eastern European parent, but there is a good chance that they won’t inherit all of the Eastern European DNA that they could potentially inherit. It’s possible for a person to share NO DNA with a great-great grandparent, even though there is a verified genealogical relationship.
Having given these questions much thought, I thought a good starting point would be to look back and start researching my own family history. When I was young I always thought I was 100% British. My Dad was born in Edgware and my mum in Hampshire. Of course, none of us are truly 100% British and as I got older I learnt that my Dad had Russian great-grandparents on one side and German on the other, and that my great grand-parents on my mother’s side were Greek. So I suppose this is when I started considering how much of my identity was defined by my family history.
The DNA tests we reviewed either require a saliva or cheek cell sample. Saliva-collecting kits include a tube that’s marked with a fill line and sample number. The tube often has a liquid-filled cap with a stabilizer that acts as a preservative to protect your DNA from degradation during transport. Cheek swab sample kits include one or two swabs for scraping the insides of your cheeks for 30 seconds to a minute to collect cheek cells and some sort of container to place the used swabs into after collection. This prevents contamination. Our testers found upsides to both types of kits but generally preferred saliva collection kits, even though they took longer.