rs121912532

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

Gene
LHCGR
Location
Chr 248,688,065 (GRCh38)
Highest magnitude
0.0Typical
Tested on
Not on consumer chips

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.0

SNPedia records rs121912532 on the minus strand: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Other LHCGR SNPs

All LHCGR SNPs

Notes

From SNPedia

Notes

Isolation of infectious bovine rhinotracheitis virus from Mustelidae. Clinical manifestations of genetic defects affecting gonadotrophins and their receptors. An update of the pathophysiology of human gonadotrophin subunit and receptor gene mutations and polymorphisms. Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor. Potential Leydig cell mitogenic signals generated by the wild-type and constitutively active mutants of the lutropin/choriogonadotropin receptor (LHR). Mutation analysis of the LH receptor gene in Leydig cell adenoma and hyperplasia and functional and biochemical studies of activating mutations of the LH receptor gene.

Source and license

Adapted from rs121912532 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.