SLC18A2, solute carrier family 18 member A2, 6571

N. diseases: 150; N. variants: 18
Disease: PARKINSONISM-DYSTONIA, INFANTILE, 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1392638187
rs1392638187
Entrez Id: 6571
Gene Symbol: SLC18A2
SLC18A2
CUI: C4747991
Disease:
PARKINSONISM-DYSTONIA, INFANTILE, 2 		0.700 GeneticVariation UNIPROT Brain dopamine-serotonin vesicular transport disease and its treatment. 23363473 2013