Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909640
rs121909640
Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0342384
Disease:
Idiopathic hypogonadotropic hypogonadism
0.010 GeneticVariation BEFREE Interestingly, the G48S mutation was identified in a normosmic IHH patient. 16882753 2006