Gene: SLC2A1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359825
rs80359825
SLC2A1
A 0.710 GeneticVariation CLINVAR

dbSNP: rs794729221
rs794729221
SLC2A1
A 0.700 CausalMutation CLINVAR Paroxysmal movement disorders in GLUT1 deficiency syndrome. 18606970

2008
dbSNP: rs1345986424
rs1345986424
SLC2A1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80359819
rs80359819
SLC2A1
T 0.700 CausalMutation CLINVAR