SLC30A10, solute carrier family 30 member 10, 55532

N. diseases: 120; N. variants: 22
Disease: Hypermanganesemia with Dystonia Polycythemia and Cirrhosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519589
rs1057519589
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1057519590
rs1057519590
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1553313783
rs1553313783
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1553313839
rs1553313839
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		G 0.700 CausalMutation CLINVAR
dbSNP: rs281860284
rs281860284
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		G 0.700 CausalMutation CLINVAR
dbSNP: rs281860285
rs281860285
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		T 0.700 CausalMutation CLINVAR
dbSNP: rs281860286
rs281860286
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		G 0.700 CausalMutation CLINVAR
dbSNP: rs281860287
rs281860287
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		G 0.700 CausalMutation CLINVAR
dbSNP: rs281860288
rs281860288
Entrez Id: 55532;107985281
Gene Symbol: SLC30A10;LOC107985281
SLC30A10;LOC107985281
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		T 0.700 CausalMutation CLINVAR
dbSNP: rs281860289
rs281860289
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		G 0.700 CausalMutation CLINVAR
dbSNP: rs281860290
rs281860290
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		A 0.700 CausalMutation CLINVAR
dbSNP: rs281860291
rs281860291
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		G 0.700 CausalMutation CLINVAR
dbSNP: rs281860292
rs281860292
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		C 0.700 CausalMutation CLINVAR
dbSNP: rs770740586
rs770740586
Entrez Id: 55532
Gene Symbol: SLC30A10
SLC30A10
CUI: C2750442
Disease:
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis 		A 0.700 CausalMutation CLINVAR