RS121908555 SCN4A

Health Risk Chr 17:63945608
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hypokalemic periodic paralysis
type 2
Hyperkalemic periodic paralysis
Inborn genetic diseases
Hypokalemic periodic paralysis
type 2
Hyperkalemic periodic paralysis
Inborn genetic diseases
Other Variants in SCN4A
rs80338957 rs80338962 rs121908544 rs121908545 rs80338958 rs121908546 rs121908556 rs80338792 rs121908547 rs121908548
Ask Dr. Hemsworth about this variant