RS121917749 SCN2A

Health Risk Chr 2:165374700
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs121917749, also known as c.3988C&gt
Associated Conditions
Seizures
benign familial infantile
3
Developmental and epileptic encephalopathy
11
Complex neurodevelopmental disorder
Seizures
benign familial infantile
3
Developmental and epileptic encephalopathy
11
Complex neurodevelopmental disorder
Other Variants in SCN2A
rs121917750 rs121917751 rs121917752 rs121917753 rs387906683 rs387906684 rs387906685 rs387906686 rs387906687 rs139815570
Ask Dr. Hemsworth about this variant