rs2313982

A SNP on chromosome 4. Its most notable genotype is G;G: common in complete genomics

Gene
None listed
Location
Chr 4137,866,906 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
8%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in complete genomicsTypical · 0.085% of people

SNPedia records rs2313982 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 11 HapMap populations.

  • AverageG;G 85%
  • European ancestry (Utah)G;G 83%
  • Han Chinese (Beijing)G;G 88%
  • Japanese (Tokyo)G;G 93%
  • Yoruba (Nigeria)G;G 74%
  • African ancestry (Southwest US)G;G 79%
  • Chinese (Denver)G;G 92%
  • Gujarati IndianG;G 94%
  • Luhya (Kenya)G;G 81%
  • Mexican ancestry (Los Angeles)G;G 90%
  • Maasai (Kenya)G;G 81%
  • TuscanG;G 83%

Notes

From SNPedia

Notes

Although an initial report in 2005 found an association between the minor allele of rs2313982 and Parkinson's disease, subsequent reports have not found any statistically significant association, most notably a meta-analysis totaling over 3,000 patients published in 2010.

Source and license

Adapted from rs2313982 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.