RS34472250 PNKP
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Associated Conditions
Microcephaly
seizures
and developmental delay
Ataxia - oculomotor apraxia type 4
Developmental and epileptic encephalopathy
12
Inborn genetic diseases
Charcot-Marie-Tooth disease type 2B2
PNKP-related disorder
Microcephaly
seizures
and developmental delay
Ataxia - oculomotor apraxia type 4
Developmental and epileptic encephalopathy
12
Other Variants in PNKP