rs4238010

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

Gene
None listed
Location
Chr 124,009,151 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
14%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableNot ratedNo summary available.Typical · 0.074% of people
  2. G;GBadHighly correlated risk factor for major depressive disorder.Typical · 0.03% of people

On SNPedia: (A;A), (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 74% G;G 3%
  • European ancestry (Utah)A;A 78% G;G 0%
  • Han Chinese (Beijing)A;A 89% G;G 0%
  • Japanese (Tokyo)A;A 91% G;G 0%
  • Yoruba (Nigeria)A;A 42% G;G 9%
  • African ancestry (Southwest US)A;A 65% G;G 5%
  • Chinese (Denver)A;A 90% G;G 0%
  • Gujarati IndianA;A 87% G;G 1%
  • Luhya (Kenya)A;A 37% G;G 13%
  • Mexican ancestry (Los Angeles)A;A 91% G;G 0%
  • Maasai (Kenya)A;A 53% G;G 8%
  • TuscanA;A 88% G;G 1%

Source and license

Adapted from rs4238010 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.