SLC2A1, solute carrier family 2 member 1, 6513

N. diseases: 687; N. variants: 76
Disease: Dystonia, Paroxysmal ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518953
rs1057518953
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1
CUI: C0393588
Disease:
Dystonia, Paroxysmal 		T 0.700 GeneticVariation CLINVAR