Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863225304
rs863225304
SLC12A5
0.800 GeneticVariation UNIPROT Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures. 26333769

2015
dbSNP: rs863225305
rs863225305
SLC12A5
0.800 GeneticVariation UNIPROT Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures. 26333769

2015
dbSNP: rs863225306
rs863225306
SLC12A5
0.800 GeneticVariation UNIPROT Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures. 26333769

2015
dbSNP: rs863225304
rs863225304
SLC12A5
C 0.800 CausalMutation CLINVAR

dbSNP: rs863225305
rs863225305
SLC12A5
A 0.800 CausalMutation CLINVAR

dbSNP: rs863225306
rs863225306
SLC12A5
A 0.800 CausalMutation CLINVAR

dbSNP: rs1220094830
rs1220094830
SLC12A5
C 0.700 CausalMutation CLINVAR

dbSNP: rs1259210706
rs1259210706
SLC12A5
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555863145
rs1555863145
SLC12A5
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555863593
rs1555863593
SLC12A5
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1555868402
rs1555868402
SLC12A5
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1568858867
rs1568858867
SLC12A5
C 0.700 CausalMutation CLINVAR

dbSNP: rs1568859798
rs1568859798
SLC12A5
T 0.700 CausalMutation CLINVAR

dbSNP: rs1568862550
rs1568862550
SLC12A5
T 0.700 CausalMutation CLINVAR

dbSNP: rs1568866916
rs1568866916
SLC12A5
T 0.700 CausalMutation CLINVAR

dbSNP: rs368484023
rs368484023
SLC12A5
G 0.700 CausalMutation CLINVAR

dbSNP: rs750336750
rs750336750
SLC12A5
T 0.700 CausalMutation CLINVAR