RS80338789 SCN4A

Health Risk Chr 17:63947091
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hypokalemic periodic paralysis
type 2
Hyperkalemic periodic paralysis
Skeletal muscle channelopathy
Hypokalemic periodic paralysis
type 2
Hyperkalemic periodic paralysis
Skeletal muscle channelopathy
Other Variants in SCN4A
rs80338957 rs80338962 rs121908544 rs121908545 rs80338958 rs121908546 rs121908556 rs80338792 rs121908547 rs121908548
Ask Dr. Hemsworth about this variant