RS1287863349 SCN4A
Upload your DNA to see your genotype for this variant.
Associated Conditions
Hypokalemic periodic paralysis
type 2
Hyperkalemic periodic paralysis
Congenital myopathy 22A
classic
Hypokalemic periodic paralysis
type 2
Hyperkalemic periodic paralysis
Congenital myopathy 22A
classic
Other Variants in SCN4A