RS1553546836 SCN1A

Health Risk Chr 2:166046874
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Associated Conditions
Autosomal dominant epilepsy
Inborn genetic diseases
Autosomal dominant epilepsy
Inborn genetic diseases
Other Variants in SCN1A
rs3812718 rs121918622 rs121918623 rs121917953 rs121917954 rs121917955 rs121917930 rs1574272192 rs121918624 rs121918625
Ask Dr. Hemsworth about this variant