rs13306747
A SNP in the PPARG gene on chromosome 3. Its most notable genotype is C;C: common in clinvar
- Gene
- PPARG
- Location
- Chr 312,416,775 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- <1%
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 4 HapMap populations.
- AverageC;C 95%
- European ancestry (Utah)C;C 100%
- Han Chinese (Beijing)C;C 93%
- Japanese (Tokyo)C;C 89%
- Yoruba (Nigeria)C;C 100%
Related
Other PPARG SNPs
- rs1801282C;GUnconfirmed higher risk of cardiovascular disease with high saturated fat dietImportant
- rs17036170A;AElevated risk for drug induced liver injury with diclofenacWorth knowing
- rs1899951C;CNo summary available.Typical
- rs2197423G;GNo summary available.Typical
- rs3856806C;Ccommon in clinvarTypical
- rs6802898C;CNo summary available.Typical
- rs17036314C;Crisk of progressing from IGT to T2D; reduced by exerciseTypical
- rs17241090C;CNo summary available.Typical
Source and license
Adapted from rs13306747 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.