| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +5 more | |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +5 more | |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +3 more | |
| | | Single nucleotide variant (intron variant) | Alternating hemiplegia of childhood 1 +5 more | |