rs12531640

A SNP in the IMMP2L gene on chromosome 7. Its most notable genotype is G;G: common on affy axiom data

Gene
IMMP2L
Location
Chr 7110,839,479 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe
Minor allele frequency
11%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon on affy axiom dataTypical · 0.079% 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 11 HapMap populations.

  • AverageG;G 79%
  • European ancestry (Utah)G;G 79%
  • Han Chinese (Beijing)G;G 75%
  • Japanese (Tokyo)G;G 74%
  • Yoruba (Nigeria)G;G 88%
  • African ancestry (Southwest US)G;G 95%
  • Chinese (Denver)G;G 76%
  • Gujarati IndianG;G 55%
  • Luhya (Kenya)G;G 97%
  • Mexican ancestry (Los Angeles)G;G 72%
  • Maasai (Kenya)G;G 91%
  • TuscanG;G 67%

Other IMMP2L SNPs

All IMMP2L SNPs

Notes

From SNPedia

Notes

non sig. gwas, hit (p = 6 x 10^-6) for intra-extra dimensional set shift (IED) EDS errors in the CANTAB (Cambridge Neuropsychological Test Automated Battery)

Source and license

Adapted from rs12531640 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.