rs2236316

A SNP in the NIN gene on chromosome 14. Its most notable genotype is G;G: common in clinvar

Gene
NIN
Location
Chr 1450,757,699 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
18%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in clinvarTypical · 0.069% of people

On SNPedia: (G;G). 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;G 69%
  • European ancestry (Utah)G;G 46%
  • Han Chinese (Beijing)G;G 71%
  • Japanese (Tokyo)G;G 68%
  • Yoruba (Nigeria)G;G 91%

Other NIN SNPs

All NIN SNPs

Source and license

Adapted from rs2236316 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.