RS199656266 SCN4A

Health Risk Chr 17:63951483
Upload your DNA to see your genotype for this variant.
Associated Conditions
Hyperkalemic periodic paralysis
Inborn genetic diseases
Congenital myasthenic syndrome 16
7 conditions
Hyperkalemic periodic paralysis
Inborn genetic diseases
Congenital myasthenic syndrome 16
7 conditions
Other Variants in SCN4A
rs80338957 rs80338962 rs121908544 rs121908545 rs80338958 rs121908546 rs121908556 rs80338792 rs121908547 rs121908548
Ask Dr. Hemsworth about this variant