RS750901301 SCN1A

Health Risk Chr 2:166039490
Upload your DNA to see your genotype for this variant.
Associated Conditions
Developmental and epileptic encephalopathy
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Early-infantile DEE
Developmental and epileptic encephalopathy
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Early-infantile DEE
Other Variants in SCN1A
rs3812718 rs121918622 rs121918623 rs121917953 rs121917954 rs121917955 rs121917930 rs1574272192 rs121918624 rs121918625
Ask Dr. Hemsworth about this variant