Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553853557
rs1553853557
Entrez Id: 1181;131408
Gene Symbol: CLCN2;FAM131A
CLCN2;FAM131A
CUI: C0020538
Disease:
Hypertensive disease
G 0.700 CausalMutation CLINVAR