Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204822
rs786204822
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271582
Disease:
Isolated lutropin deficiency (disorder)
A 0.700 CausalMutation CLINVAR
dbSNP: rs786204822
rs786204822
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271582
Disease:
Isolated lutropin deficiency (disorder)
G 0.700 CausalMutation CLINVAR