| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130060218, VAMP2 (S28G +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC130060218, VAMP2 (P10A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130060218, VAMP2 (P22L +1 more) | Single nucleotide variant (missense variant) | VAMP2-related disorder | |
| | LOC130060218, VAMP2 (A3V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130060218, VAMP2 (A5T +1 more) | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements | |
| | LOC130060218, VAMP2 (P13S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130060218, VAMP2 (A21fs +1 more) | Deletion (frameshift variant) | Neurodevelopmental disorder | |
| | LOC130060218, VAMP2 (P13L +1 more) | Single nucleotide variant (missense variant) | not provided | |
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