RS794726839 SCN1A

Health Risk Chr 2:165992290
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What This Variant Does
"CLNSIG=5
Associated Conditions
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Other Variants in SCN1A
rs3812718 rs121918622 rs121918623 rs121917953 rs121917954 rs121917955 rs121917930 rs1574272192 rs121918624 rs121918625
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