Gene: SLC2A1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909739
rs121909739
SLC2A1
T 0.810 CausalMutation CLINVAR

dbSNP: rs121909740
rs121909740
SLC2A1
T 0.800 CausalMutation CLINVAR

dbSNP: rs202060209
rs202060209
SLC2A1
A 0.800 CausalMutation CLINVAR

dbSNP: rs267607060
rs267607060
SLC2A1
AT 0.800 CausalMutation CLINVAR

dbSNP: rs267607061
rs267607061
SLC2A1
A 0.800 CausalMutation CLINVAR

dbSNP: rs80359818
rs80359818
SLC2A1
A 0.800 CausalMutation 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: rs80359826
rs80359826
SLC2A1
A 0.700 CausalMutation CLINVAR Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome. 10980529

2000
dbSNP: rs13306758
rs13306758
SLC2A1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553156047
rs1553156047
SLC2A1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557646867
rs1557646867
SLC2A1
CT 0.700 CausalMutation CLINVAR

dbSNP: rs794727870
rs794727870
SLC2A1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs796053248
rs796053248
SLC2A1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80359812
rs80359812
SLC2A1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80359825
rs80359825
SLC2A1
A 0.700 CausalMutation CLINVAR