RS121918624 SCN1A

Health Risk Chr 2:166052882
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What This Variant Does
"[OMIM:?]
Associated Conditions
Severe myoclonic epilepsy in infancy
Migraine
familial hemiplegic
3
Generalized epilepsy with febrile seizures plus
type 2
Intellectual disability
Inborn genetic diseases
Developmental and epileptic encephalopathy 6B
Febrile seizures
familial
3a
Early-infantile DEE
Severe myoclonic epilepsy in infancy
Migraine
Other Variants in SCN1A
rs3812718 rs121918622 rs121918623 rs121917953 rs121917954 rs121917955 rs121917930 rs1574272192 rs121918625 rs121918626
Ask Dr. Hemsworth about this variant