RS796052860 PNKP
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Developmental and epileptic encephalopathy
12
Developmental and epileptic encephalopathy
12
Inborn genetic diseases
Developmental and epileptic encephalopathy
12
Developmental and epileptic encephalopathy
12
Other Variants in PNKP