RS756127631 SCN8A

Health Risk Chr 12:51769127
Upload your DNA to see your genotype for this variant.
Associated Conditions
Cognitive impairment with or without cerebellar ataxia
Seizures
benign familial infantile
5
Developmental and epileptic encephalopathy
13
Early-infantile DEE
Cognitive impairment with or without cerebellar ataxia
Seizures
benign familial infantile
5
Developmental and epileptic encephalopathy
13
Early-infantile DEE
Other Variants in SCN8A
rs202151337 rs397514738 rs117217073 rs587780453 rs201458257 rs587780454 rs587780455 rs587780586 rs587777721 rs587777722
Ask Dr. Hemsworth about this variant