rs10490625

A SNP in the INSIG2 gene on chromosome 2. Its most notable genotype is G;G: common in complete genomics

Gene
INSIG2
Location
Chr 2118,101,980 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe
Minor allele frequency
5%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in complete genomicsTypical · 0.093% of people

SNPedia records rs10490625 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 9 HapMap populations.

  • AverageG;G 93%
  • European ancestry (Utah)G;G 85%
  • Han Chinese (Beijing)G;G 99%
  • Japanese (Tokyo)G;G 97%
  • Yoruba (Nigeria)G;G 97%
  • African ancestry (Southwest US)G;G 98%
  • Chinese (Denver)G;G 97%
  • Gujarati IndianG;G 87%
  • Mexican ancestry (Los Angeles)G;G 88%
  • TuscanG;G 85%

Other INSIG2 SNPs

All INSIG2 SNPs

Source and license

Adapted from rs10490625 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.