rs11636232
A SNP in the HERC2 gene on chromosome 15. Its most notable genotype is T;T: lighter eye color
- Gene
- HERC2
- Location
- Chr 1528,141,480 (GRCh38)
- Highest magnitude
- 1.0Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 15%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageC;C 85% T;T 2%
- European ancestry (Utah)C;C 34% T;T 13%
- Han Chinese (Beijing)C;C 100% T;T 0%
- Japanese (Tokyo)C;C 100% T;T 0%
- Yoruba (Nigeria)C;C 100% T;T 0%
- African ancestry (Southwest US)C;C 81% T;T 2%
- Chinese (Denver)C;C 99% T;T 0%
- Gujarati IndianC;C 97% T;T 0%
- Mexican ancestry (Los Angeles)C;C 85% T;T 2%
- TuscanC;C 71% T;T 3%
Related
Source and license
Adapted from rs11636232 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.