SLC1A2, solute carrier family 1 member 2, 6506

N. diseases: 208; N. variants: 12
Disease: Amyotrophic Lateral Sclerosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs377633002
rs377633002
Entrez Id: 6506
Gene Symbol: SLC1A2
SLC1A2
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis 		0.010 GeneticVariation BEFREE The A79G sequence variant was not found in 55 patients with ALS or in 50 non-neurological controls. 9771796 1998