RS199676994 SCN4A

Health Risk Chr 17:63968107
Upload your DNA to see your genotype for this variant.
Associated Conditions
Congenital myasthenic syndrome 16
Potassium-aggravated myotonia
Paramyotonia congenita of Von Eulenburg
Hypokalemic periodic paralysis
type 2
Inborn genetic diseases
Hyperkalemic periodic paralysis
Congenital myasthenic syndrome 16
Potassium-aggravated myotonia
Paramyotonia congenita of Von Eulenburg
Hypokalemic periodic paralysis
type 2
Inborn genetic diseases
Hyperkalemic periodic paralysis
Other Variants in SCN4A
rs80338957 rs80338962 rs121908544 rs121908545 rs80338958 rs121908546 rs121908556 rs80338792 rs121908547 rs121908548
Ask Dr. Hemsworth about this variant