Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs750281602
rs750281602
SLC39A14
0.800 GeneticVariation UNIPROT Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia. 27231142

2016
dbSNP: rs879253763
rs879253763
SLC39A14
0.800 GeneticVariation UNIPROT Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia. 27231142

2016
dbSNP: rs879253766
rs879253766
SLC39A14
0.800 GeneticVariation UNIPROT Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia. 27231142

2016
dbSNP: rs750281602
rs750281602
SLC39A14
G 0.800 CausalMutation CLINVAR

dbSNP: rs879253763
rs879253763
SLC39A14
G 0.800 CausalMutation CLINVAR

dbSNP: rs879253766
rs879253766
SLC39A14
A 0.800 CausalMutation CLINVAR

dbSNP: rs1039778197
rs1039778197
SLC39A14
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554519011
rs1554519011
SLC39A14
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554519303
rs1554519303
SLC39A14
A 0.700 CausalMutation CLINVAR

dbSNP: rs879253764
rs879253764
SLC39A14
T 0.700 CausalMutation CLINVAR

dbSNP: rs879253765
rs879253765
SLC39A14
T 0.700 CausalMutation CLINVAR