rs272889
A SNP in the SLC22A4 gene on chromosome 5. Its most notable genotype is A;G: common in complete genomics
- Gene
- SLC22A4
- Location
- Chr 5132,329,685 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 41%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs272889 on the minus strand: (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageA;G 42%
- European ancestry (Utah)A;G 52%
- Han Chinese (Beijing)A;G 48%
- Japanese (Tokyo)A;G 37%
- Yoruba (Nigeria)A;G 35%
- African ancestry (Southwest US)A;G 33%
- Chinese (Denver)A;G 52%
- Gujarati IndianA;G 43%
- Luhya (Kenya)A;G 33%
- Mexican ancestry (Los Angeles)A;G 52%
- Maasai (Kenya)A;G 39%
- TuscanA;G 39%
Related
Other SLC22A4 SNPs
- rs1050152T;T2.1x increased risk of Crohn's diseaseWorth knowing
- rs12777C;Ccommon in complete genomicsTypical
- rs272879C;Gcommon in complete genomicsTypical
- rs272893C;Tcommon in complete genomicsTypical
- rs2073838G;GNo summary available.Typical
- rs3792876C;CNo summary available.Typical
- rs11568500G;Gcommon in complete genomicsTypical
- rs11568506G;Gcommon in complete genomicsTypical
Source and license
Adapted from rs272889 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.