RS80338955 SCN4A

Health Risk Chr 17:63957473
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hyperkalemic periodic paralysis
Paramyotonia congenita of Von Eulenburg
Hyperkalemic periodic paralysis
Paramyotonia congenita of Von Eulenburg
Other Variants in SCN4A
rs80338957 rs80338962 rs121908544 rs121908545 rs80338958 rs121908546 rs121908556 rs80338792 rs121908547 rs121908548
Ask Dr. Hemsworth about this variant