SLC12A3, solute carrier family 12 member 3, 6559

N. diseases: 252; N. variants: 131
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909385
rs121909385
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
C 0.820 CausalMutation CLINVAR
dbSNP: rs200697179
rs200697179
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
G 0.820 CausalMutation CLINVAR
dbSNP: rs121909382
rs121909382
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
T 0.810 CausalMutation CLINVAR
dbSNP: rs28936388
rs28936388
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
T 0.810 CausalMutation CLINVAR
dbSNP: rs775931992
rs775931992
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
T 0.810 CausalMutation CLINVAR
dbSNP: rs121909379
rs121909379
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs121909380
rs121909380
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
A 0.800 CausalMutation CLINVAR
dbSNP: rs121909380
rs121909380
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
T 0.800 CausalMutation CLINVAR
dbSNP: rs121909383
rs121909383
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
T 0.800 CausalMutation CLINVAR
dbSNP: rs121909384
rs121909384
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
T 0.800 CausalMutation CLINVAR
dbSNP: rs202114767
rs202114767
Entrez Id: 6559;102466752
Gene Symbol: SLC12A3;MIR6863
SLC12A3;MIR6863
CUI: C0268450
Disease:
Gitelman Syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs28936387
rs28936387
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs34803727
rs34803727
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs752101663
rs752101663
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
A 0.800 CausalMutation CLINVAR
dbSNP: rs752101663
rs752101663
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
0.800 GeneticVariation UNIPROT
dbSNP: rs148038173
rs148038173
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
0.710 GeneticVariation UNIPROT
dbSNP: rs200817545
rs200817545
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
T 0.710 CausalMutation CLINVAR
dbSNP: rs753523115
rs753523115
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
0.710 GeneticVariation UNIPROT
dbSNP: rs886039754
rs886039754
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
G 0.710 GeneticVariation CLINVAR
dbSNP: rs1231715433
rs1231715433
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
0.700 GeneticVariation UNIPROT
dbSNP: rs1298687889
rs1298687889
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
0.700 GeneticVariation UNIPROT
dbSNP: rs13306668
rs13306668
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1375515522
rs1375515522
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
0.700 GeneticVariation UNIPROT
dbSNP: rs1380031877
rs1380031877
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
0.700 GeneticVariation UNIPROT
dbSNP: rs148945966
rs148945966
Entrez Id: 6559
Gene Symbol: SLC12A3
SLC12A3
CUI: C0268450
Disease:
Gitelman Syndrome
0.700 GeneticVariation UNIPROT