rs7900909
A SNP in the LOC105378334 gene on chromosome 10. Its most notable genotype is T;T: common in complete genomics
- Gene
- LOC105378334
- Location
- Chr 1064,688,715 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 24%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 10 HapMap populations.
- AverageT;T 56%
- European ancestry (Utah)T;T 74%
- Han Chinese (Beijing)T;T 45%
- Japanese (Tokyo)T;T 33%
- Yoruba (Nigeria)T;T 63%
- Chinese (Denver)T;T 50%
- Gujarati IndianT;T 43%
- Luhya (Kenya)T;T 53%
- Mexican ancestry (Los Angeles)T;T 51%
- Maasai (Kenya)T;T 72%
- TuscanT;T 73%
Source and license
Adapted from rs7900909 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.