RS760270633 DNM1

Health Risk Chr 9:128220201
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
31A
Inborn genetic diseases
Developmental and epileptic encephalopathy
31A
Inborn genetic diseases
Other Variants in DNM1
rs587777860 rs587777861 rs587777862 rs1554774401 rs869312702 rs754404446 rs1057518655 rs1057524561 rs527412689 rs546517702
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