| | | Single nucleotide variant (missense variant +2 more) | Migraine, familial hemiplegic, 3 +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Migraine, familial hemiplegic, 3 +3 more | |
| | LOC102724058, SCN1A (D1726N +5 more) | Single nucleotide variant (missense variant +1 more) | Severe myoclonic epilepsy in infancy +3 more | |
| | | Duplication (splice donor variant) | Severe myoclonic epilepsy in infancy +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Migraine, familial hemiplegic, 3 | |
| | LOC102724058, SCN1A (R1613G +5 more) | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 | |
| | | Single nucleotide variant (missense variant +2 more) | Migraine, familial hemiplegic, 3 | |
| | | Single nucleotide variant (splice donor variant) | Migraine, familial hemiplegic, 3 | |
| | | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 | |
| | | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +3 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Severe myoclonic epilepsy in infancy +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Migraine, familial hemiplegic, 3 +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Migraine, familial hemiplegic, 3 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Migraine, familial hemiplegic, 3 +4 more | GPathogenic/Likely pathogenic |
| | LOC102724058, SCN1A (T1127K +5 more) | Single nucleotide variant (missense variant +1 more) | Early infantile epileptic encephalopathy with suppression bursts | |
| | LOC102724058, SCN1A (W1423R +5 more) | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 +4 more | |
| | | Single nucleotide variant (nonsense +2 more) | Migraine, familial hemiplegic, 3 +4 more | |
| | LOC102724058, SCN1A (G1148S +5 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | |
| | LOC102724058, SCN1A (L1328P +5 more) | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 | |
| | LOC102724058, SCN1A (K1580I +5 more) | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 | |
| | | Deletion (splice donor variant) | Migraine, familial hemiplegic, 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Migraine, familial hemiplegic, 3 | |
| | | Indel (frameshift variant +2 more) | Migraine, familial hemiplegic, 3 | |
| | | Single nucleotide variant (nonsense +2 more) | Migraine, familial hemiplegic, 3 | |
| | | Single nucleotide variant (nonsense +2 more) | Migraine, familial hemiplegic, 3 | |
| | LOC102724058, SCN1A (L1634S +5 more) | Single nucleotide variant (missense variant +1 more) | Early infantile epileptic encephalopathy with suppression bursts +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | LOC102724058, SCN1A (Y1753H +5 more) | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | |
| | | Insertion (intron variant) | Migraine, familial hemiplegic, 3 | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Early infantile epileptic encephalopathy with suppression bursts +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | |
| | LOC102724058, SCN1A (N1153K +5 more) | Single nucleotide variant (missense variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | |
| | | Single nucleotide variant (intron variant) | Early infantile epileptic encephalopathy with suppression bursts +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +3 more) | Generalized epilepsy with febrile seizures plus, type 2 +3 more | |
| | LOC102724058, SCN1A (R1379Q +5 more) | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Migraine, familial hemiplegic, 3 +1 more | |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 3 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +1 more | |
| | | Duplication (frameshift variant +2 more) | Early infantile epileptic encephalopathy with suppression bursts | |
| | LOC102724058, SCN1A (E1670K +5 more) | Single nucleotide variant (missense variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Early infantile epileptic encephalopathy with suppression bursts +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | LOC102724058, SCN1A (N1350I +5 more) | Single nucleotide variant (missense variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Early infantile epileptic encephalopathy with suppression bursts +5 more | |
| | | Single nucleotide variant (nonsense +2 more) | not provided +4 more | |
| | LOC102724058, SCN1A (K1401E +5 more) | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Generalized epilepsy with febrile seizures plus, type 2 +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | Early infantile epileptic encephalopathy with suppression bursts +4 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Early infantile epileptic encephalopathy with suppression bursts +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Generalized epilepsy with febrile seizures plus, type 2 +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Generalized epilepsy with febrile seizures plus, type 2 +4 more | GConflicting classifications of pathogenicity |
| | LOC102724058, SCN1A (K1985N +5 more) | Single nucleotide variant (missense variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | LOC102724058, SCN1A (R1901* +5 more) | Single nucleotide variant (nonsense +1 more) | Migraine, familial hemiplegic, 3 +3 more | |
| | LOC102724058, SCN1A (V1527I +5 more) | Single nucleotide variant (missense variant +1 more) | Early infantile epileptic encephalopathy with suppression bursts +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Generalized epilepsy with febrile seizures plus, type 2 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | LOC102724058, SCN1A (A1940S +5 more) | Single nucleotide variant (missense variant +1 more) | Migraine, familial hemiplegic, 3 +5 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Early infantile epileptic encephalopathy with suppression bursts +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Early infantile epileptic encephalopathy with suppression bursts +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Early infantile epileptic encephalopathy with suppression bursts +3 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy +2 more | |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 3 +4 more | GConflicting classifications of pathogenicity |
| | | Duplication (intron variant) | not specified +7 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Inborn genetic diseases +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Epilepsy +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Migraine, familial hemiplegic, 3 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Migraine, familial hemiplegic, 3 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +5 more | |
| | | Single nucleotide variant (intron variant) | Early infantile epileptic encephalopathy with suppression bursts +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | LOC102724058, SCN1A (E1998Q +5 more) | Single nucleotide variant (missense variant +1 more) | Early infantile epileptic encephalopathy with suppression bursts +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Epilepsy +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Epilepsy +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Epilepsy +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Generalized epilepsy with febrile seizures plus, type 2 +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Epilepsy +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Epilepsy +2 more | |