Gene: SLC2A1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13306758
rs13306758
SLC2A1
A 0.800 GeneticVariation CLINVAR

dbSNP: rs13306758
rs13306758
SLC2A1
A 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs387907313
rs387907313
SLC2A1
A 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs397514564
rs397514564
SLC2A1
G 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs398123069
rs398123069
SLC2A1
C 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs796053272
rs796053272
SLC2A1
C 0.700 CausalMutation CLINVAR Clinical utility of genetic testing in pediatric drug-resistant epilepsy: a pilot study. 25108116

2014
dbSNP: rs1557646867
rs1557646867
SLC2A1
CT 0.700 CausalMutation CLINVAR

dbSNP: rs796053248
rs796053248
SLC2A1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80359825
rs80359825
SLC2A1
A 0.700 CausalMutation CLINVAR