rs7656250

A SNP in the PPARGC1A gene on chromosome 4. Its most notable genotype is T;T: common in complete genomics

Gene
PPARGC1A
Location
Chr 423,864,393 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
27%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in complete genomicsTypical · 0.057% of people

On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageT;T 57%
  • European ancestry (Utah)T;T 55%
  • Han Chinese (Beijing)T;T 42%
  • Japanese (Tokyo)T;T 30%
  • Yoruba (Nigeria)T;T 86%
  • African ancestry (Southwest US)T;T 77%
  • Chinese (Denver)T;T 46%
  • Gujarati IndianT;T 33%
  • Luhya (Kenya)T;T 86%
  • Mexican ancestry (Los Angeles)T;T 46%
  • Maasai (Kenya)T;T 77%
  • TuscanT;T 45%

Other PPARGC1A SNPs

All PPARGC1A SNPs

Source and license

Adapted from rs7656250 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.