RS199975643 SCN3A

Health Risk Chr 2:165140667
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Associated Conditions
Developmental and epileptic encephalopathy
62
Epilepsy
familial focal
with variable foci 4
Inborn genetic diseases
Developmental and epileptic encephalopathy
62
Epilepsy
familial focal
with variable foci 4
Inborn genetic diseases
Other Variants in SCN3A
rs748935500 rs575814709 rs144957412 rs138766015 rs200538599 rs797044933 rs145171998 rs199597878 rs746501220 rs370141420
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