RS1057518801 SCN3A

Health Risk Chr 2:165130238
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Polymicrogyria
Developmental delay
Developmental and epileptic encephalopathy
62
Epilepsy
familial focal
with variable foci 4
Polymicrogyria
Developmental delay
Developmental and epileptic encephalopathy
62
Epilepsy
familial focal
with variable foci 4
Other Variants in SCN3A
rs748935500 rs575814709 rs199975643 rs144957412 rs138766015 rs200538599 rs797044933 rs145171998 rs199597878 rs746501220
Ask Dr. Hemsworth about this variant