| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (synonymous variant) | GLUT1 deficiency syndrome 1, autosomal recessive +8 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +7 more | |
| | | Deletion (intron variant) | GLUT1 deficiency syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +7 more | |
| | | Single nucleotide variant (intron variant) | Encephalopathy due to GLUT1 deficiency +7 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +8 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +8 more | |
| | | Single nucleotide variant (synonymous variant) | Childhood onset GLUT1 deficiency syndrome 2 +7 more | |
Click to view in NCBI Gene