rs1800067

A SNP in the ERCC4 gene on chromosome 16. Its most notable genotype is A;G.

Gene
ERCC4
Location
Chr 1613,935,176 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
3%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;GMost notableNot ratedNo summary available.Typical · 0.05% of people
  2. G;GGoodcommon in complete genomicsTypical · 0.095% of people

On SNPedia: (A;G), (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.

  • AverageA;G 5% G;G 95%
  • European ancestry (Utah)A;G 8% G;G 91%
  • Han Chinese (Beijing)A;G 0% G;G 100%
  • Japanese (Tokyo)A;G 0% G;G 100%
  • Yoruba (Nigeria)A;G 0% G;G 100%
  • African ancestry (Southwest US)A;G 4% G;G 97%
  • Chinese (Denver)A;G <1% G;G 99%
  • Gujarati IndianA;G 6% G;G 94%
  • Luhya (Kenya)A;G <1% G;G 99%
  • Mexican ancestry (Los Angeles)A;G 9% G;G 91%
  • Maasai (Kenya)A;G 10% G;G 90%
  • TuscanA;G 17% G;G 83%

Other ERCC4 SNPs

All ERCC4 SNPs

Source and license

Adapted from rs1800067 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.