rs642698

A SNP in the ME2 gene on chromosome 18. Its most notable genotype is G;T.

Gene
ME2
Location
Chr 1850,896,615 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe
Minor allele frequency
31%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;TMost notableNot ratedNo summary available.Typical · 0.00% of people

SNPedia records rs642698 on the minus strand: (A;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;T 0%
  • European ancestry (Utah)G;T 0%
  • Han Chinese (Beijing)G;T 0%
  • Japanese (Tokyo)G;T 0%
  • Yoruba (Nigeria)G;T 0%
  • African ancestry (Southwest US)G;T 0%
  • Chinese (Denver)G;T 0%
  • Gujarati IndianG;T 0%
  • Luhya (Kenya)G;T 0%
  • Mexican ancestry (Los Angeles)G;T 0%
  • Maasai (Kenya)G;T 0%
  • TuscanG;T 0%

Conditions, medicines and genes

Notes

From SNPedia

Notes

pubmedcentral.nih.gov May Underlie Susceptibility to Adolescent-Onset Idiopathic Generalized Epilepsy

Source and license

Adapted from rs642698 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.