RS1235665641 SCN4A

Health Risk Chr 17:63966171
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Associated Conditions
Inborn genetic diseases
Hyperkalemic periodic paralysis
7 conditions
Congenital myopathy 22A
classic
Inborn genetic diseases
Hyperkalemic periodic paralysis
7 conditions
Congenital myopathy 22A
classic
Other Variants in SCN4A
rs80338957 rs80338962 rs121908544 rs121908545 rs80338958 rs121908546 rs121908556 rs80338792 rs121908547 rs121908548
Ask Dr. Hemsworth about this variant