RS1554776842 STXBP1

Health Risk Chr 9:127660080
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Associated Conditions
Inborn genetic diseases
Infantile epilepsy syndrome
Inborn genetic diseases
Infantile epilepsy syndrome
Other Variants in STXBP1
rs121918317 rs121918318 rs121918319 rs121918320 rs121918321 rs587776641 rs398123695 rs587777310 rs201809337 rs147607230
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