RS200611702 PNKP

Health Risk Chr 19:49861634
Upload your DNA to see your genotype for this variant.
Associated Conditions
Microcephaly
seizures
and developmental delay
Developmental and epileptic encephalopathy
12
Ataxia - oculomotor apraxia type 4
Inborn genetic diseases
Microcephaly
seizures
and developmental delay
Developmental and epileptic encephalopathy
12
Ataxia - oculomotor apraxia type 4
Inborn genetic diseases
Other Variants in PNKP
rs267606956 rs587784365 rs267606957 rs374745816 rs376854895 rs116192442 rs148491228 rs201503405 rs144284975 rs151180981
Ask Dr. Hemsworth about this variant