rs13405728

A SNP in the LHCGR gene on chromosome 2. Its most notable genotype is A;A: common in complete genomics

Gene
LHCGR
Location
Chr 248,751,020 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
20%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in complete genomicsTypical · 0.062% of people

On SNPedia: (A;A). 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;A 62%
  • European ancestry (Utah)A;A 90%
  • Han Chinese (Beijing)A;A 59%
  • Japanese (Tokyo)A;A 42%
  • Yoruba (Nigeria)A;A 45%
  • African ancestry (Southwest US)A;A 61%
  • Chinese (Denver)A;A 52%
  • Gujarati IndianA;A 74%
  • Luhya (Kenya)A;A 46%
  • Mexican ancestry (Los Angeles)A;A 60%
  • Maasai (Kenya)A;A 64%
  • TuscanA;A 88%

Other LHCGR SNPs

All LHCGR SNPs

Notes

From SNPedia

Notes

Association of polycystic ovary syndrome susceptibility single nucleotide polymorphism rs2479106 and PCOS in Caucasian patients with PCOS or hirsutism as referral diagnosis. Variants in DENND1A Are Associated with Polycystic Ovary Syndrome in Women of European Ancestry.

Source and license

Adapted from rs13405728 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.