rs237885

A SNP in the OXTR gene on chromosome 3. Its most notable genotype is G;T: common in complete genomics

Gene
OXTR
Location
Chr 38,753,857 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
45%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;TMost notableGoodcommon in complete genomicsTypical · 0.045% of people

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

Frequency

Share of each genotype in 4 HapMap populations.

  • AverageG;T 45%
  • European ancestry (Utah)G;T 54%
  • Han Chinese (Beijing)G;T 44%
  • Japanese (Tokyo)G;T 31%
  • Yoruba (Nigeria)G;T 51%

Other OXTR SNPs

All OXTR SNPs

Source and license

Adapted from rs237885 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.