| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (non-coding transcript variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (non-coding transcript variant) | GLUT1 deficiency syndrome +1 more | |
| | | Single nucleotide variant (non-coding transcript variant) | Epilepsy, idiopathic generalized, susceptibility to, 12 +7 more | |
| | | Single nucleotide variant (non-coding transcript variant) | GLUT1 deficiency syndrome +1 more | |
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