rs3734016
A SNP in the ERAP1 gene on chromosome 5. Its most notable genotype is C;C: common on affy axiom data
- Gene
- ERAP1
- Location
- Chr 596,803,761 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 9%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3734016 on the minus strand: (G;G). 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.
- AverageC;C 83%
- European ancestry (Utah)C;C 94%
- Han Chinese (Beijing)C;C 69%
- Japanese (Tokyo)C;C 59%
- Yoruba (Nigeria)C;C 86%
- African ancestry (Southwest US)C;C 83%
- Chinese (Denver)C;C 71%
- Gujarati IndianC;C 92%
- Luhya (Kenya)C;C 90%
- Mexican ancestry (Los Angeles)C;C 75%
- Maasai (Kenya)C;C 97%
- TuscanC;C 95%
Related
Other ERAP1 SNPs
- rs30187T;T2x higher risk for Ankylosing Spondylitis.Worth knowing
- rs10050860T;THalf the risk (about 0.05%) of Ankylosing Spondylitis.Minor
- rs2549782G;G1.6x increased risk for preeclampsia in most populationsMinor
- rs27044C;Cnormal riskTypical
- rs2287987C;C0.71x lower risk for spondylitisTypical
- rs17408150T;Tcommon on affy axiom dataTypical
- rs17482078C;C0.76x lower risk for spondylitisTypical
Source and license
Adapted from rs3734016 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.