rs1324694
A SNP in the ERLIN1 gene on chromosome 10. Its most notable genotype is C;C: common in complete genomics
- Gene
- ERLIN1
- Location
- Chr 10100,186,688 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 7%
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 8 HapMap populations.
- AverageC;C 80%
- European ancestry (Utah)C;C 99%
- Han Chinese (Beijing)C;C 84%
- Japanese (Tokyo)C;C 83%
- Yoruba (Nigeria)C;C 71%
- African ancestry (Southwest US)C;C 76%
- Chinese (Denver)C;C 76%
- Gujarati IndianC;C 85%
- Luhya (Kenya)C;C 63%
Source and license
Adapted from rs1324694 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.