rs17036170
A SNP in the PPARG gene on chromosome 3. Its most notable genotype is A;A: Elevated risk for drug induced liver injury with diclofenac
- Gene
- PPARG
- Location
- Chr 312,288,912 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- <1%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadElevated risk for drug induced liver injury with diclofenac
- A;GBadIncreased risk of drug induced liver injury with diclofenac
- G;GGoodcommon/normal
On SNPedia: (A;A), (A;G), (G;G). 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.
- AverageA;A 4% A;G 96% G;G 0%
- European ancestry (Utah)A;A <1% A;G 99% G;G 0%
- African ancestry (Southwest US)A;A 2% A;G 98% G;G 0%
- Mexican ancestry (Los Angeles)A;A 6% A;G 94% G;G 0%
- TuscanA;A 7% A;G 93% G;G 0%
Related
Other PPARG SNPs
- rs1801282C;GUnconfirmed higher risk of cardiovascular disease with high saturated fat dietImportant
- 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
- rs17241090C;CNo summary available.Typical
Notes
From SNPedia
Notes
A;A
This uncommon risk allele A was found in a GWAS to be associated with drug induced liver injury with diclofenac. OR = 11.3 (4.9–25.9) Replicability is uncertain, but individuals with this genotype should be aware of the potential of increased risk. The odds ratio above is probably for heterozygotes, and it is not clear if the homozygous AA is worse, if in fact the risk can be replicated.
A;G
This uncommon risk allele A was found in a GWAS to be associated with drug induced liver injury with diclofenac. OR = 11.3 (4.9–25.9) Replicability is uncertain, but individuals with this genotype should be aware of the potential of increased risk.
Source and license
Adapted from rs17036170 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.