rs9326506

A SNP in the ZNF239 gene on chromosome 10. Its most notable genotype is A;A.

Gene
ZNF239
Location
Chr 1043,573,110 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
45%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableNot ratedNo summary available.Typical · 0.043% of people
  2. A;CNot rated1.3x riskTypical · 0.041% of people
  3. C;CNot ratednormalTypical · 0.016% of people
  4. T;TNot ratedNo summary available.Typical · 0.00% of people

On SNPedia: (A;A), (A;C), (C;C), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 8 HapMap populations.

  • AverageA;A 43% A;C 41% C;C 16% T;T 0%
  • European ancestry (Utah)A;A 29% A;C 48% C;C 23% T;T 0%
  • Han Chinese (Beijing)A;A 19% A;C 49% C;C 32% T;T 0%
  • Japanese (Tokyo)A;A 16% A;C 52% C;C 32% T;T 0%
  • Yoruba (Nigeria)A;A 64% A;C 34% C;C 2% T;T 0%
  • African ancestry (Southwest US)A;A 59% A;C 29% C;C 13% T;T 0%
  • Chinese (Denver)A;A 22% A;C 58% C;C 20% T;T 0%
  • Luhya (Kenya)A;A 71% A;C 25% C;C 4% T;T 0%
  • Maasai (Kenya)A;A 65% A;C 34% C;C <1% T;T 0%

Conditions, medicines and genes

Notes

From SNPedia

Notes

rs9326506 has been reported in a large study to be associated with type-2 diabetes. The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.28 (CI 1.11-1.48), and for homozygotes, 1.46 (CI 1.24-1.72).

A;A

normal

Source and license

Adapted from rs9326506 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.