RS1841564743 STXBP1

Health Risk Chr 9:127672075
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Associated Conditions
Infantile epilepsy syndrome
Inborn genetic diseases
Infantile epilepsy syndrome
Inborn genetic diseases
Other Variants in STXBP1
rs121918317 rs121918318 rs121918319 rs121918320 rs121918321 rs587776641 rs398123695 rs587777310 rs201809337 rs147607230
Ask Dr. Hemsworth about this variant