rs5030980
A SNP in the ATP6V0D1 gene on chromosome 16. Its most notable genotype is C;C: common in complete genomics
- Gene
- ATP6V0D1
- Location
- Chr 1667,483,042 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 2%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs5030980 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 7 HapMap populations.
- AverageC;C 94%
- European ancestry (Utah)C;C 94%
- African ancestry (Southwest US)C;C 95%
- Gujarati IndianC;C 98%
- Luhya (Kenya)C;C 96%
- Mexican ancestry (Los Angeles)C;C 98%
- Maasai (Kenya)C;C 82%
- TuscanC;C 91%
Source and license
Adapted from rs5030980 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.