rs467323

A SNP in the AQP2 gene on chromosome 12. Its most notable genotype is C;C: common in clinvar

Gene
AQP2
Location
Chr 1249,955,982 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
43%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.041% of people

SNPedia records rs467323 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 5 HapMap populations.

  • AverageC;C 41%
  • European ancestry (Utah)C;C 5%
  • Han Chinese (Beijing)C;C 62%
  • Japanese (Tokyo)C;C 59%
  • Yoruba (Nigeria)C;C 71%
  • TuscanC;C 9%

Other AQP2 SNPs

All AQP2 SNPs

Source and license

Adapted from rs467323 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.