rs238417

A SNP in the ERCC2 gene on chromosome 19. Its most notable genotype is G;G: common in clinvar

Gene
ERCC2
Location
Chr 1945,353,210 (GRCh38)
Highest magnitude
0.0Typical
Tested on
Not on consumer chips

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in clinvarTypical · 0.015% of people

SNPedia records rs238417 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 4 HapMap populations.

  • AverageG;G 15%
  • European ancestry (Utah)G;G 10%
  • Han Chinese (Beijing)G;G 28%
  • Japanese (Tokyo)G;G 23%
  • Yoruba (Nigeria)G;G 0%

Other ERCC2 SNPs

All ERCC2 SNPs

Source and license

Adapted from rs238417 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.