rs1540771
A SNP in the LOC105374875 gene on chromosome 6. Its most notable genotype is T;T: common in complete genomics
- Gene
- LOC105374875
- Location
- Chr 6466,033 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 35%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs1540771 on the minus strand: (A;A). 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.
- AverageT;T 11%
- European ancestry (Utah)T;T 26%
- Han Chinese (Beijing)T;T 5%
- Japanese (Tokyo)T;T 12%
- Yoruba (Nigeria)T;T 0%
- African ancestry (Southwest US)T;T 5%
- Chinese (Denver)T;T 8%
- Gujarati IndianT;T 13%
- Luhya (Kenya)T;T <1%
- Mexican ancestry (Los Angeles)T;T 22%
- Maasai (Kenya)T;T 3%
- TuscanT;T 24%
Related
Other LOC105374875 SNPs
Notes
From SNPedia
Notes
plos the association between rs12203592 and hair color was independent of rs1540771, a SNP between the IRF4 and EXOC2 genes previously found to be associated with hair color.
Source and license
Adapted from rs1540771 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.