Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909385
rs121909385
SLC12A3
C 0.820 CausalMutation CLINVAR

dbSNP: rs200697179
rs200697179
SLC12A3
G 0.820 CausalMutation CLINVAR

dbSNP: rs121909382
rs121909382
SLC12A3
T 0.810 CausalMutation CLINVAR

dbSNP: rs28936388
rs28936388
SLC12A3
T 0.810 CausalMutation CLINVAR

dbSNP: rs775931992
rs775931992
SLC12A3
T 0.810 CausalMutation CLINVAR

dbSNP: rs121909379
rs121909379
SLC12A3
C 0.800 CausalMutation CLINVAR

dbSNP: rs121909380
rs121909380
SLC12A3
A 0.800 CausalMutation CLINVAR

dbSNP: rs121909380
rs121909380
SLC12A3
T 0.800 CausalMutation CLINVAR

dbSNP: rs121909383
rs121909383
SLC12A3
T 0.800 CausalMutation CLINVAR

dbSNP: rs121909384
rs121909384
SLC12A3
T 0.800 CausalMutation CLINVAR

dbSNP: rs202114767
rs202114767
SLC12A3 ; MIR6863
A 0.800 GeneticVariation CLINVAR

dbSNP: rs28936387
rs28936387
SLC12A3
C 0.800 CausalMutation CLINVAR

dbSNP: rs34803727
rs34803727
SLC12A3
A 0.800 GeneticVariation CLINVAR

dbSNP: rs752101663
rs752101663
SLC12A3
A 0.800 CausalMutation CLINVAR

dbSNP: rs752101663
rs752101663
SLC12A3
0.800 GeneticVariation UNIPROT

dbSNP: rs148038173
rs148038173
SLC12A3
0.710 GeneticVariation UNIPROT

dbSNP: rs200817545
rs200817545
SLC12A3
T 0.710 CausalMutation CLINVAR

dbSNP: rs753523115
rs753523115
SLC12A3
0.710 GeneticVariation UNIPROT

dbSNP: rs886039754
rs886039754
SLC12A3
G 0.710 GeneticVariation CLINVAR

dbSNP: rs1231715433
rs1231715433
SLC12A3
0.700 GeneticVariation UNIPROT

dbSNP: rs1298687889
rs1298687889
SLC12A3
0.700 GeneticVariation UNIPROT

dbSNP: rs13306668
rs13306668
SLC12A3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1375515522
rs1375515522
SLC12A3
0.700 GeneticVariation UNIPROT

dbSNP: rs1380031877
rs1380031877
SLC12A3
0.700 GeneticVariation UNIPROT

dbSNP: rs148945966
rs148945966
SLC12A3
0.700 GeneticVariation UNIPROT