RS121917995 SCN1A

Health Risk Chr 2:165992368
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What This Variant Does
"CLNSIG=5
Associated Conditions
Macrocephaly and epileptic encephalopathy
Inborn genetic diseases
Migraine
familial hemiplegic
3
Severe myoclonic epilepsy in infancy
Early-infantile DEE
Developmental and epileptic encephalopathy 6B
Severe myoclonic epilepsy in infancy
SCN1A-related disorder
Early-infantile DEE
Macrocephaly and epileptic encephalopathy
Inborn genetic diseases
Migraine
familial hemiplegic
Other Variants in SCN1A
rs3812718 rs121918622 rs121918623 rs121917953 rs121917954 rs121917955 rs121917930 rs1574272192 rs121918624 rs121918625
Ask Dr. Hemsworth about this variant