rs10131

A SNP in the LIG4 gene on chromosome 13. Its most notable genotype is T;T.

Gene
LIG4
Location
Chr 13108,207,498 (GRCh38)
Highest magnitude
0.0Typical
Tested on
AncestryDNA, FamilyTreeDNA
Minor allele frequency
11%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableNot ratedNo summary available.Typical · 0.01% of people
  2. C;TNot ratedNo summary available.Typical · 0.021% of people
  3. C;CGoodcommon in clinvarTypical · 0.078% of people

SNPedia records rs10131 on the minus strand: (A;A), (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 5 HapMap populations.

  • AverageT;T 1% C;T 21% C;C 78%
  • European ancestry (Utah)T;T 3% C;T 14% C;C 83%
  • Han Chinese (Beijing)T;T 0% C;T 22% C;C 78%
  • Japanese (Tokyo)T;T 0% C;T 29% C;C 71%
  • Yoruba (Nigeria)T;T 0% C;T 22% C;C 78%
  • Chinese (Denver)T;T 3% C;T 19% C;C 78%

Other LIG4 SNPs

All LIG4 SNPs

Notes

From SNPedia

Notes

Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer PMC2851649

Source and license

Adapted from rs10131 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.