Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs515726224
rs515726224
Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0342384
Disease:
Idiopathic hypogonadotropic hypogonadism
T 0.700 CausalMutation CLINVAR Congenital hypogonadotropic hypogonadism during childhood: presentation and genetic analyses in 46 boys. 24204987 2013