rs1566667

A SNP on chromosome 12. Its most notable genotype is A;A.

Gene
None listed
Location
Chr 12130,127,245 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
23%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableNot ratedNo summary available.Typical · 0.08% of people
  2. A;GNot ratedNo summary available.Typical · 0.038% of people
  3. G;GNot ratedNo summary available.Typical · 0.054% of people

On SNPedia: (A;A), (A;G), (G;G). 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.

  • AverageA;A 8% A;G 38% G;G 54%
  • European ancestry (Utah)A;A 2% A;G 19% G;G 80%
  • Han Chinese (Beijing)A;A 7% A;G 43% G;G 51%
  • Japanese (Tokyo)A;A 4% A;G 34% G;G 63%
  • Yoruba (Nigeria)A;A 12% A;G 51% G;G 36%
  • African ancestry (Southwest US)A;A 9% A;G 52% G;G 39%
  • Chinese (Denver)A;A 7% A;G 44% G;G 48%
  • Gujarati IndianA;A 11% A;G 44% G;G 45%
  • Luhya (Kenya)A;A 21% A;G 49% G;G 30%
  • Mexican ancestry (Los Angeles)A;A 3% A;G 17% G;G 79%
  • Maasai (Kenya)A;A 15% A;G 41% G;G 44%
  • TuscanA;A 2% A;G 20% G;G 78%

Notes

From SNPedia

Notes

This SNP, rs1566667, was mentioned as one of the SNPs defining a haplotype used during a search for a deafness-associated gene on chromosome 12. However, rs1566667 itself has no reported associations with deafness (or any other condition).

Source and license

Adapted from rs1566667 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.