rs1110061

A SNP in the NR5A1 gene on chromosome 9. Its most notable genotype is C;C: common in clinvar

Gene
NR5A1
Location
Chr 9124,500,523 (GRCh38)
Highest magnitude
0.0Typical
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.00% of people
  2. C;GGoodbenign polymorphismTypical · 0.00% of people
  3. G;GGoodNo summary available.Typical · 0.0100% of people

On SNPedia: (C;C), (C;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 2 HapMap populations.

  • AverageC;C 0% C;G 0% G;G 100%
  • European ancestry (Utah)C;C 0% C;G 0% G;G 100%
  • Yoruba (Nigeria)C;C 0% C;G 0% G;G 100%

Source and license

Adapted from rs1110061 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.