Gene entry
LHCGR
luteinizing hormone/choriogonadotropin receptor
- Chromosome
- 2
- Cytoband
- 2p16.3
- Variants (rsID)
- 26
LHCGR is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p16.3). Its official name is “luteinizing hormone/choriogonadotropin receptor”. The reference table lists 26 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs2293275Benignsingle nucleotide variantHypergonadotropic hypogonadism|Gonadotropin-independent familial sexual precocity|Leydig cell agenesis
- rs121912525Pathogenicsingle nucleotide variantLeydig hypoplasia, type I
- rs121912530Pathogenicsingle nucleotide variantLeydig cell hypoplasia, type II
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.