| | | Single nucleotide variant (missense variant) | Hypokalemic periodic paralysis, type 2 | |
| | | Single nucleotide variant (missense variant) | Hypokalemic periodic paralysis, type 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Hypokalemic periodic paralysis, type 2 | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +1 more | |
| | | Single nucleotide variant (missense variant) | Hypokalemic periodic paralysis, type 2 | |
| | | Single nucleotide variant (missense variant) | Potassium-aggravated myotonia +4 more | |
| | | Single nucleotide variant (missense variant) | Potassium-aggravated myotonia +4 more | |
| | | Single nucleotide variant (intron variant) | Potassium-aggravated myotonia +5 more | |
| | | Deletion (intron variant) | Potassium-aggravated myotonia +5 more | |
| | | Single nucleotide variant (intron variant) | Potassium-aggravated myotonia +5 more | |
| | | Single nucleotide variant (synonymous variant) | Congenital myasthenic syndrome 16 +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (synonymous variant) | Congenital myasthenic syndrome 16 +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (synonymous variant) | Congenital myasthenic syndrome 16 +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (synonymous variant) | Congenital myasthenic syndrome 16 +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +7 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +7 more | |
| | | Single nucleotide variant (missense variant) | Congenital myasthenic syndrome 16 +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Congenital myasthenic syndrome 16 +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Hypokalemic periodic paralysis, type 2 | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Hypokalemic periodic paralysis, type 2 +7 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Microsatellite (inframe_deletion) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (synonymous variant) | Hypokalemic periodic paralysis, type 1 +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hypokalemic periodic paralysis, type 1 +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hypokalemic periodic paralysis, type 1 +6 more | |
| | | Single nucleotide variant (missense variant) | Congenital myasthenic syndrome 16 +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Congenital myasthenic syndrome 16 +6 more | |
| | | Single nucleotide variant (missense variant) | Paramyotonia congenita of Von Eulenburg +5 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +7 more | |
| | | Single nucleotide variant (missense variant) | Congenital myasthenic syndrome 16 +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Potassium-aggravated myotonia +5 more | |
| | | Single nucleotide variant (missense variant) | not specified +7 more | |
| | | Single nucleotide variant (synonymous variant) | Potassium-aggravated myotonia +5 more | |
| | | Single nucleotide variant (missense variant) | not specified +6 more | |
| | | Single nucleotide variant (missense variant) | SCN4A-related condition +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +6 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (missense variant) | Hyperkalemic periodic paralysis +5 more | |
| | | Single nucleotide variant (intron variant) | Hyperkalemic periodic paralysis +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Congenital myasthenic syndrome 16 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Congenital myasthenic syndrome 16 +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital myasthenic syndrome 16 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Congenital myasthenic syndrome 16 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital myasthenic syndrome 16 +4 more | |