|Summary||Mitochondrial Haplogroup H1f|
This is the genoset for a mitochondrial DNA haplogroup. H1f is a subclade of H1. It is found in Northern Europe and reaches its highest frequency in Finland.
H1f is defined by four SNPs, T4452C, T7309C, A9066G, and T16093C. Because 16093 has an extremely high mutation rate it is excluded from the matching criteria.
- Defining SNPs for H1
- G3010A, rs3928306(A;A)
H1 status is confirmed using genoset 1002.
As 16093 has a high mutation rate it will be excluded from the criteria. The rest is going to be set to require at least two of the first three SNPs.
and( gs1002, i3002167(C;C), i4000743(C;C), i4000650(G;G), )