Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs970697573
rs970697573
Entrez Id: 9170
Gene Symbol: LPAR2
LPAR2
CUI: C0271623
Disease:
Hypogonadotropic hypogonadism
0.010 GeneticVariation BEFREE Partially inactivating substitutions of the GnRHR frequently found in familial hypogonadotrophic hypogonadism are Q106R and R262Q. 23155690 2012