rs805264

A SNP in the APOM gene on chromosome 6. Its most notable genotype is G;G: common in complete genomics

Gene
APOM
Location
Chr 631,656,096 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
7%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in complete genomicsTypical · 0.083% of people

SNPedia records rs805264 on the minus strand: (C;C). 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 83%
  • European ancestry (Utah)G;G 97%
  • Han Chinese (Beijing)G;G 73%
  • Japanese (Tokyo)G;G 89%
  • Yoruba (Nigeria)G;G 72%
  • African ancestry (Southwest US)G;G 72%
  • Chinese (Denver)G;G 68%
  • Gujarati IndianG;G 92%
  • Luhya (Kenya)G;G 77%
  • Mexican ancestry (Los Angeles)G;G 90%
  • Maasai (Kenya)G;G 85%
  • TuscanG;G 93%

Other APOM SNPs

All APOM SNPs

Notes

From SNPedia

Notes

C allele of rs805297 was significantly associated with T2D duration of longer than 10 years (OR?=?1.245, p?=?0.015).

Source and license

Adapted from rs805264 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.