rs1799801

A SNP in the ERCC4 gene on chromosome 16. Its most notable genotype is T;T: common in clinvar

Gene
ERCC4
Location
Chr 1613,948,101 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
23%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in clinvarTypical · 0.059% of people

On SNPedia: (T;T). 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.

  • AverageT;T 59%
  • European ancestry (Utah)T;T 61%
  • Han Chinese (Beijing)T;T 58%
  • Japanese (Tokyo)T;T 48%
  • Yoruba (Nigeria)T;T 82%
  • African ancestry (Southwest US)T;T 72%
  • Chinese (Denver)T;T 63%
  • Gujarati IndianT;T 47%
  • Luhya (Kenya)T;T 58%
  • Mexican ancestry (Los Angeles)T;T 66%
  • Maasai (Kenya)T;T 41%
  • TuscanT;T 55%

Other ERCC4 SNPs

All ERCC4 SNPs

Notes

From SNPedia

Notes

Genetic polymorphisms in the nucleotide excision repair pathway and lung cancer risk: a meta-analysis. Polymorphisms in DNA repair genes, smoking, and bladder cancer risk: findings from the international consortium of bladder cancer.

Source and license

Adapted from rs1799801 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.