Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs769066903
rs769066903
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271582
Disease:
Isolated lutropin deficiency (disorder)
T 0.700 CausalMutation CLINVAR