rs3807153

A SNP in the ATP6V0A4 gene on chromosome 7. Its most notable genotype is A;G: carrier of a benign change

Gene
ATP6V0A4
Location
Chr 7138,733,046 (GRCh38)
Highest magnitude
1.0Minor
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
8%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GGoodbenignTypical · 0.13% of people
  2. A;GMost notableGoodcarrier of a benign changeMinor · 1.018% of people
  3. A;AGoodnormalTypical · 0.080% of people

SNPedia records rs3807153 on the minus strand: (C;C), (C;T), (T;T). 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.

  • AverageG;G 3% A;G 18% A;A 80%
  • European ancestry (Utah)G;G 0% A;G 5% A;A 95%
  • Han Chinese (Beijing)G;G 2% A;G 8% A;A 91%
  • Japanese (Tokyo)G;G 0% A;G 12% A;A 88%
  • Yoruba (Nigeria)G;G 4% A;G 25% A;A 71%
  • African ancestry (Southwest US)G;G 4% A;G 23% A;A 74%
  • Chinese (Denver)G;G 0% A;G 6% A;A 94%
  • Gujarati IndianG;G 1% A;G 24% A;A 75%
  • Luhya (Kenya)G;G 9% A;G 42% A;A 49%
  • Mexican ancestry (Los Angeles)G;G 2% A;G 4% A;A 95%
  • Maasai (Kenya)G;G 7% A;G 40% A;A 54%
  • TuscanG;G 0% A;G 6% A;A 94%

Other ATP6V0A4 SNPs

All ATP6V0A4 SNPs

Notes

From SNPedia

Notes

G;G

This has been reported in another database to be associated with kidney issues. However, this genotype has been seen in several SNPedians, including User:Razib and User:Ronald Bailey, and no one has reported any consequences so far.

Source and license

Adapted from rs3807153 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.