Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852704
rs137852704
SCNN1B
T 0.700 CausalMutation CLINVAR Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome. 27900368

2016
dbSNP: rs1293789661
rs1293789661
CLCN2
T 0.700 CausalMutation CLINVAR

dbSNP: rs138977195
rs138977195
SLC12A3
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553856214
rs1553856214
CLCN2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555206402
rs1555206402
HMBS
A 0.700 CausalMutation CLINVAR

dbSNP: rs200817545
rs200817545
SLC12A3
T 0.700 CausalMutation CLINVAR

dbSNP: rs758379595
rs758379595
CLCN2
T 0.700 CausalMutation CLINVAR