Disease: LIDDLE SYNDROME 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853342
rs137853342
Entrez Id: 6340
Gene Symbol: SCNN1G
SCNN1G
CUI: C4748251
Disease:
LIDDLE SYNDROME 2 		A 0.700 CausalMutation CLINVAR