SLC2A1, solute carrier family 2 member 1, 6513

N. diseases: 687; N. variants: 76
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13306758
rs13306758
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1
CUI: C3553859
Disease:
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 		A 0.800 GeneticVariation CLINVAR
dbSNP: rs13306758
rs13306758
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1
CUI: C3553859
Disease:
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 		0.800 GeneticVariation UNIPROT
dbSNP: rs13306758
rs13306758
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1
CUI: C3553859
Disease:
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 		A 0.800 SusceptibilityMutation CLINVAR