RS121918738 SCN1A

Health Risk Chr 2:166013820
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Generalized epilepsy with febrile seizures plus
Early-infantile DEE
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Generalized epilepsy with febrile seizures plus
Early-infantile DEE
Other Variants in SCN1A
rs3812718 rs121918622 rs121918623 rs121917953 rs121917954 rs121917955 rs121917930 rs1574272192 rs121918624 rs121918625
Ask Dr. Hemsworth about this variant