I have previously written about beginning my DNA adventures with a test with 23andMe, a company that focuses more on the health aspects of genetics than the genealogical aspects. They had an offer I couldn’t refuse, and I didn’t!
When I got up this morning there was an email to say that my genetic profile was ready. I had to go out and so couldn’t give this interesting news the attention that it deserved, until now. I’d like to write down my impressions as I go through the results.
The menu is split into three headings:
- My Health
- My Ancestry
- Sharing and Community
The first thing I did before I left the house this morning was look for my mtDNA haplotype under My Ancestry. This is the one that sorts you into migration groups from 10-50,000 years ago. Mine is X2b:
According to 23andMe haplogroup X2 is mostly found in southern Europe, Central Asia, and North America, with a few scattered populations in places like the Orkney Islands in Scotland. It is relatively rare in most of the populations in which it is found.
It’s nice to think that my haplogroup is relatively rare. We all like to think of ourselves as a bit special! I can trace my direct female line back five generations to Agnes Allan, who married William Stewart in Paisley, Scotland, in 1827, and died before William remarried and took his family to Auckland, New Zealand in 1842. So perhaps she was descended from the people who ended up in Orkney.
Other headings under My Ancestry are:
- Relative Finder, which won’t have results for another week or so. Disappointing!
- Paternal Line which is no good to me since I am not male and the paternal line can only be traced by the Y chromosome, which women do not have.
- Ancestry Painting, which makes no sense to me at the moment. It has a diagram of some chromosomes and a key that shows different colours meaning different things if the chromosomes show those colours. My chromosomes show no colours, only grey bits, and apparently “Gray segments indicate regions where 23andMe’s genotyping chip has no markers.”
- Global Similarity shows your similarity to groups of people from around the world. Check it out:
I am slightly more similar to the people of Oceania than to any of the Europeans. Apparently Oceania includes the people of Australia (ie, Aboriginals), New Guinea and the Pacific Islands, including New Zealand, but the sample only includes those from New Guinea. The sample dates from January 2008, which is a bit disappointing.
There is the opportunity to see the graph for others who have shared their profile with you, and those I can see have predominantly Northern Europeans and very little Oceania. That makes sense. Most of us in Australia, aside from the Aboriginal people, come from Europe.
My father, however, is a part-European Fijian. The Fijians are Melanesian, with some Polynesian where they associated with people from Tonga and other islands. So this result makes some sense.
When I have some time I will delve into these results in more detail to work out how they arrive at the conclusions they have.
Under the heading Sharing and Community are the tools for comparing your genes with those of relatives. So far I have shared my profile with two people, and I have no similarities with either of them. I will look at this category in more detail when it has something to show me.
The first heading, which I have left until last, is My Health. First up is Disease Risk.
The results for Parkinson’s Disease are locked, so that they can explain what the results mean, and don’t mean, before you see them. I think that’s a good idea. I have a scientific background and know that the percentages they are talking about are very small, but others may be unnecessarily concerned.
The other results are displayed in a long list, with the increased risk first, followed by decreased risk and then typical risk. The ones on the top of my list are no more than double the very low average incidence, which is heartening. I can then click on each one to find out more. Here are some of my ‘typical risks’:
Where the results show a red and green arrow there are multiple markers associated with the condition, and I may have one or more of them.
It would be easy, I imagine, to use these results as an excuse to do nothing. If I see a graph that shows my risk of heart attack is greater than average I might resign myself to the fact and keep living on fatty foods and no exercise (which I don’t – it’s hypothetical). Or I could make some changes to counteract the predisposition in my genes.
Each item on the list also gives a ‘confidence rating’, the stars, based on the number of studies that have been done and the number of participants in the studies.
I have a slightly higher risk of developing asthma, based on one of three markers for which studies have been done. The studies are listed and described, with the type of population and numbers of subjects described. I actually do suffer from asthma.
Carrier status to certain conditions has a similar layout. I’ll have a good look at that later.
Drug response will also take some time to digest. I am likely to be a fast metaboliser of caffeine, which I gave up some years ago, and I have typical results for most other items on the list.
Traits looks interesting. I don’t have the muscle performance of a world-class sprinter, nor am I resistant to malaria or HIV/AIDS. I am likely to have brown eyes (correct) and to have straighter hair (correct, despite my father having frizzy black hair).
That’s enough for now. It will take some time to go into this more thoroughly. My initial reaction is positive, and I’m glad I spent the $99.