RS879255699 SCN8A

Health Risk Chr 12:51705510
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
13
Inborn genetic diseases
Developmental and epileptic encephalopathy
13
Inborn genetic diseases
Other Variants in SCN8A
rs202151337 rs397514738 rs117217073 rs587780453 rs201458257 rs587780454 rs587780455 rs587780586 rs587777721 rs587777722
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