rs17408150
A SNP in the ERAP1 gene on chromosome 5. Its most notable genotype is T;T: common on affy axiom data
- Gene
- ERAP1
- Location
- Chr 596,903,554 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 2%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). 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.
- AverageT;T 98%
- European ancestry (Utah)T;T 92%
- Han Chinese (Beijing)T;T 100%
- Japanese (Tokyo)T;T 100%
- Yoruba (Nigeria)T;T 100%
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
- rs3734016C;Ccommon on affy axiom dataTypical
- rs17482078C;C0.76x lower risk for spondylitisTypical
Source and license
Adapted from rs17408150 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.