rs17241090
A SNP in the PPARG gene on chromosome 3. Its most notable genotype is C;C.
- Gene
- PPARG
- Location
- Chr 312,351,626 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
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 10 HapMap populations.
- AverageC;C 90%
- European ancestry (Utah)C;C 82%
- Han Chinese (Beijing)C;C 89%
- Japanese (Tokyo)C;C 95%
- Yoruba (Nigeria)C;C 100%
- African ancestry (Southwest US)C;C 95%
- Chinese (Denver)C;C 94%
- Gujarati IndianC;C 83%
- Mexican ancestry (Los Angeles)C;C 79%
- Maasai (Kenya)C;C 97%
- TuscanC;C 86%
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
- rs13306747C;Ccommon in clinvarTypical
- rs17036314C;Crisk of progressing from IGT to T2D; reduced by exerciseTypical
Source and license
Adapted from rs17241090 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.