rs2705293
A SNP in the LOC401478 gene on chromosome 8. Its most notable genotype is T;T: common in complete genomics
- Gene
- LOC401478
- Location
- Chr 8137,906,702 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 12%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2705293 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 76%
- European ancestry (Utah)T;T 86%
- Han Chinese (Beijing)T;T 85%
- Japanese (Tokyo)T;T 91%
- Yoruba (Nigeria)T;T 57%
- African ancestry (Southwest US)T;T 58%
- Chinese (Denver)T;T 95%
- Gujarati IndianT;T 90%
- Luhya (Kenya)T;T 47%
- Mexican ancestry (Los Angeles)T;T 90%
- Maasai (Kenya)T;T 56%
- TuscanT;T 85%
Notes
From SNPedia
Notes
rs9291683, rs3129934 and rs2705293 discussed in the context of CNVs in a blog post
Source and license
Adapted from rs2705293 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.