rs9514067

A SNP in the ERCC5 gene on chromosome 13. Its most notable genotype is C;C: common in complete genomics

Gene
ERCC5
Location
Chr 13102,875,580 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
<1%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in complete genomicsTypical · 0.099% of people
  2. G;GGoodcommon in clinvarTypical · 0.00% of people

On SNPedia: (C;C), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 3 HapMap populations.

  • AverageC;C 99% G;G 0%
  • Han Chinese (Beijing)C;C 100% G;G 0%
  • Japanese (Tokyo)C;C 100% G;G 0%
  • Yoruba (Nigeria)C;C 97% G;G 0%

Other ERCC5 SNPs

All ERCC5 SNPs

Source and license

Adapted from rs9514067 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.