| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (splice donor variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 +1 more | |
| | ATP1A2, LOC126805890 (S220L) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 +2 more | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies +5 more | |
| | | Single nucleotide variant (intron variant) | Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies +5 more | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +4 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 2 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Migraine, familial hemiplegic, 2 +7 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies +4 more | |
| | | Duplication (intron variant) | Alternating hemiplegia of childhood 1 +5 more | |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 2 +5 more | |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 2 +5 more | |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine +1 more | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Deletion (frameshift variant) | Alternating hemiplegia of childhood +1 more | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (3 prime UTR variant) | Migraine, familial hemiplegic, 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Developmental and epileptic encephalopathy 98 +4 more | |
| | | Single nucleotide variant (intron variant) | Alternating hemiplegia of childhood 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Alternating hemiplegia of childhood 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | ATP1A2, LOC126805890 (T224I) | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 2 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 +2 more | |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 2 | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial hemiplegic migraine +2 more | |
| | | Deletion | Variegate porphyria +3 more | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine +6 more | |
| | | Single nucleotide variant (intron variant) | Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine +6 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +6 more | |
| | ATP1A2, LOC126805890 (N246D) | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Migraine, familial hemiplegic, 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | ATP1A2-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | Familial hemiplegic migraine +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Familial hemiplegic migraine +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +4 more | |
| | | Single nucleotide variant (intron variant) | Alternating hemiplegia of childhood 1 +5 more | |
| | | Single nucleotide variant (intron variant) | Familial hemiplegic migraine +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Alternating hemiplegia of childhood 1 +5 more | |
| | | Single nucleotide variant (synonymous variant) | Alternating hemiplegia of childhood 1 +7 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +7 more | |
| | | Single nucleotide variant (synonymous variant) | Alternating hemiplegia of childhood 1 +6 more | |
| | | Single nucleotide variant (synonymous variant) | Developmental and epileptic encephalopathy 98 +5 more | |