RS144957412 SCN3A

Health Risk Chr 2:165127771
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Associated Conditions
Epilepsy
familial focal
with variable foci 4
Developmental and epileptic encephalopathy
62
Inborn genetic diseases
Epilepsy
familial focal
with variable foci 4
Developmental and epileptic encephalopathy
62
Inborn genetic diseases
Other Variants in SCN3A
rs748935500 rs575814709 rs199975643 rs138766015 rs200538599 rs797044933 rs145171998 rs199597878 rs746501220 rs370141420
Ask Dr. Hemsworth about this variant