RS80338958 SCN4A

Health Risk Chr 17:63945614
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What This Variant Does
"[OMIM:?]
Associated Conditions
Paramyotonia congenita/hyperkalemic periodic paralysis
Hyperkalemic periodic paralysis
Focal-onset seizure
6 conditions
Inborn genetic diseases
SCN4A-related disorder
Potassium-aggravated myotonia
Paramyotonia congenita/hyperkalemic periodic paralysis
Hyperkalemic periodic paralysis
Focal-onset seizure
6 conditions
Inborn genetic diseases
SCN4A-related disorder
Potassium-aggravated myotonia
Other Variants in SCN4A
rs80338957 rs80338962 rs121908544 rs121908545 rs121908546 rs121908556 rs80338792 rs121908547 rs121908548 rs121908549
Ask Dr. Hemsworth about this variant