Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397509434
rs397509434
Entrez Id: 3291
Gene Symbol: HSD11B2
HSD11B2
CUI: C3887949
Disease:
Apparent mineralocorticoid excess
C 0.700 CausalMutation CLINVAR