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Both the other options would give me much less information than what I already have, and, accordingly, a lower resolution on my maternal “haplogroup” (genetic family). The first option (129 dollars) only reads 22 SNPs (point mutations) in the so-called Hipervariable Region 1 (HVR1), which is like looking at the mtDNA with a simple magnifying glass; the second one (189 dollars), adds to that a series of SNPs from Hipervariable Region 2 (HVR2), which gives a somewhat higher resolution. But compare this to the data from 23andme, which reads some 3,000 SNPs not only from HVR1 and 2, but also along the rest of the whole mtDNA molecule. I rest my case. The advantage of FTDNA, though, is that it’s been around longer and has many more clients than 23andme, which means many more people with whom to compare our results in search of similarities.
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