rs1805034

A SNP in the TNFRSF11A gene on chromosome 18. Its most notable genotype is C;C: common in clinvar

Gene
TNFRSF11A
Location
Chr 1862,360,008 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
40%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.015% of people

On SNPedia: (C;C). 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.

  • AverageC;C 15%
  • European ancestry (Utah)C;C 30%
  • Han Chinese (Beijing)C;C 17%
  • Japanese (Tokyo)C;C 10%
  • Yoruba (Nigeria)C;C 16%
  • African ancestry (Southwest US)C;C 12%
  • Chinese (Denver)C;C 10%
  • Gujarati IndianC;C 28%
  • Luhya (Kenya)C;C 4%
  • Mexican ancestry (Los Angeles)C;C 7%
  • Maasai (Kenya)C;C 6%
  • TuscanC;C 26%

Other TNFRSF11A SNPs

All TNFRSF11A SNPs

Notes

From SNPedia

Notes

Association analyses suggest the effects of RANK and RANKL on age at menarche in Chinese women.

Source and license

Adapted from rs1805034 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.