So I am apparently 2.8% Neandertal, slightly more than the average amongst Europeans. I am also in mitochondrial DNA subclade J1c3b1, which is part of a loooooong line of Neolithic farmers and herders who arose in the Near East 8-10K years ago and are associated with the spread of agriculture into Europe. All on my mom's side. No telling what's on my dad's side as all my near male relatives are now dead, and as I lack a Y chromosome, there's certain tests they can't do. :) (Edit: According to 23andMe, the J1 subtype is primarily British and Scandinavian. As my grandfather belonged to Clan Fraser, color me not surprised. XD Although it's mitochondrial DNA, so it really didn't come from him, but from my maternal grandmother, who was English through and through.)
My health results also tell me, among others, that I have an elevated risk of migraines (duh) and of Dupuytren's contracture, which I knew because my mom has that. (Edit: That condition is also known among Viking-descended peoples...again, color me not surprised.)
There are no major surprises, which is good to know, actually: you can learn if you're a carrier of some of the major mutations involved in increased risk of breast cancer, Alzheimer's, Parkinson's, etc. They hide those results away so you can choose whether or not to view them, and you have to read a report before looking at them that emphasizes this is RISK and STATISTICS, not a definite yes or no.
I'm really interested in seeing what the National Geographic results will be--they focus on deep ancestry, over thousands of years, while 23andMe tends to go for health-related stuff.
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