rs2070951

A SNP in the NR3C2 gene on chromosome 4. Its most notable genotype is G;G: common in clinvar

Gene
NR3C2
Location
Chr 4148,436,862 (GRCh38)
Highest magnitude
0.0Typical
Tested on
AncestryDNA
Minor allele frequency
49%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in clinvarTypical · 0.028% of people

SNPedia records rs2070951 on the minus strand: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 10 HapMap populations.

  • AverageG;G 28%
  • European ancestry (Utah)G;G 32%
  • Han Chinese (Beijing)G;G 7%
  • Japanese (Tokyo)G;G 12%
  • Yoruba (Nigeria)G;G 69%
  • African ancestry (Southwest US)G;G 51%
  • Chinese (Denver)G;G 4%
  • Gujarati IndianG;G 8%
  • Mexican ancestry (Los Angeles)G;G 11%
  • Maasai (Kenya)G;G 63%
  • TuscanG;G 28%

Other NR3C2 SNPs

All NR3C2 SNPs

Source and license

Adapted from rs2070951 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.