rs703556
A SNP in the LOC105369944 gene on chromosome 12. Its most notable genotype is A;A: common genotype
- Gene
- LOC105369944
- Location
- Chr 12102,618,116 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs703556 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 9 HapMap populations.
- AverageA;A 89%
- European ancestry (Utah)A;A 97%
- Han Chinese (Beijing)A;A 74%
- Japanese (Tokyo)A;A 81%
- Yoruba (Nigeria)A;A 100%
- Chinese (Denver)A;A 73%
- Gujarati IndianA;A 89%
- Mexican ancestry (Los Angeles)A;A 91%
- Maasai (Kenya)A;A 99%
- TuscanA;A 96%
Related
Source and license
Adapted from rs703556 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.