rs908327
A SNP in the LOC101927851 gene on chromosome 1. Its most notable genotype is A;A: common genotype
- Gene
- LOC101927851
- Location
- Chr 1234,956,853 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 2%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs908327 on the minus strand: (T;T). 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.
- AverageA;A 95%
- European ancestry (Utah)A;A 100%
- Han Chinese (Beijing)A;A 100%
- Japanese (Tokyo)A;A 100%
- Yoruba (Nigeria)A;A 85%
- African ancestry (Southwest US)A;A 93%
- Luhya (Kenya)A;A 87%
- Mexican ancestry (Los Angeles)A;A 97%
- Maasai (Kenya)A;A 97%
Source and license
Adapted from rs908327 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.