RS796053361 STXBP1

Health Risk Chr 9:127668160
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
4
Inborn genetic diseases
Infantile epilepsy syndrome
Early-infantile DEE
Inborn genetic diseases
Infantile epilepsy syndrome
Developmental and epileptic encephalopathy
4
Developmental and epileptic encephalopathy
4
Inborn genetic diseases
Infantile epilepsy syndrome
Early-infantile DEE
Inborn genetic diseases
Other Variants in STXBP1
rs121918317 rs121918318 rs121918319 rs121918320 rs121918321 rs587776641 rs398123695 rs587777310 rs201809337 rs147607230
Ask Dr. Hemsworth about this variant