RS587777848 KCNB1

Health Risk Chr 20:49374519
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
26
Inborn genetic diseases
Neurodevelopmental delay
Developmental and epileptic encephalopathy
26
Epileptic encephalopathy
Developmental and epileptic encephalopathy
26
Inborn genetic diseases
Neurodevelopmental delay
Developmental and epileptic encephalopathy
26
Epileptic encephalopathy
Other Variants in KCNB1
rs587777849 rs587777850 rs886039396 rs886041743 rs886041617 rs1057518621 rs947355756 rs761452916 rs1057524688 rs565025643
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