RS121918318 STXBP1

Health Risk Chr 9:127663314
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What This Variant Does
"[OMIM:?]
Associated Conditions
Developmental and epileptic encephalopathy
4
Inborn genetic diseases
Developmental and epileptic encephalopathy
4
Inborn genetic diseases
Other Variants in STXBP1
rs121918317 rs121918319 rs121918320 rs121918321 rs587776641 rs398123695 rs587777310 rs201809337 rs147607230 rs587784455
Ask Dr. Hemsworth about this variant