|Summary||Mitochondrial Haplogroup H1b|
This is the genoset for a mitochondrial DNA haplogroup. H1b is a predominately European subclade of H1.
H1b is defined by three mutations. A3796G, T16189C, and T16356C. The C value for 16356 is not tested by the 23andMe V2 chip. Because it frequently back mutates, T16189C is excluded from the matching criteria. Therefor this genoset only requires matching with previous criteria for H1 and A3796G.
- Defining SNPs for H1
- G3010A, rs3928306(A;A)
H1 status is confirmed using genoset 1002.
This will only require A3796G.
and( gs1002, rs3928306(A;A), or(rs28357970(G;G), i3002114(G;G)), )