rs17650401
A SNP in the PPARGC1A gene on chromosome 4. Its most notable genotype is C;C: common genotype
- Gene
- PPARGC1A
- Location
- Chr 424,374,210 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA
- Minor allele frequency
- 3%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 7 HapMap populations.
- AverageC;C 96%
- European ancestry (Utah)C;C 83%
- Han Chinese (Beijing)C;C 100%
- Japanese (Tokyo)C;C 100%
- Yoruba (Nigeria)C;C 100%
- African ancestry (Southwest US)C;C 98%
- Gujarati IndianC;C 99%
- TuscanC;C 94%
Related
Other PPARGC1A SNPs
- rs2290602G;T2.7x increased risk for nonalcoholic fatty liver diseaseWorth knowing
- rs3736265G;GNo summary available.Typical
- rs3774923C;CNo summary available.Typical
- rs7656250T;Tcommon in complete genomicsTypical
- rs8192678T;Thigher blood pressure if <50Typical
- rs13117172C;Ccommon in complete genomicsTypical
Source and license
Adapted from rs17650401 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.