rs2072134

A SNP in the OAS3 gene on chromosome 12. Its most notable genotype is G;G: common in complete genomics

Gene
OAS3
Location
Chr 12112,971,371 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
4%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in complete genomicsTypical · 0.083% of people
  2. C;CNot ratedNo summary available.Typical · 0.00% of people

SNPedia records rs2072134 on the minus strand: (C;C), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 5 HapMap populations.

  • AverageG;G 83% C;C 0%
  • European ancestry (Utah)G;G 100% C;C 0%
  • Han Chinese (Beijing)G;G 76% C;C 0%
  • Japanese (Tokyo)G;G 66% C;C 0%
  • Yoruba (Nigeria)G;G 100% C;C 0%
  • Chinese (Denver)G;G 71% C;C 0%

Other OAS3 SNPs

All OAS3 SNPs

Source and license

Adapted from rs2072134 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.