rs9285640
A SNP in the PPARGC1B gene on chromosome 5. Its most notable genotype is G;G: common genotype
- Gene
- PPARGC1B
- Location
- Chr 5149,762,504 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA
- Minor allele frequency
- 3%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 3 HapMap populations.
- AverageG;G 100%
- European ancestry (Utah)G;G 99%
- Han Chinese (Beijing)G;G 100%
- Japanese (Tokyo)G;G 100%
Related
Source and license
Adapted from rs9285640 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.