RS796052862 PNKP

Health Risk Chr 19:49861672
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
12
Charcot-Marie-Tooth disease type 2B2
Inborn genetic diseases
Developmental and epileptic encephalopathy
12
Charcot-Marie-Tooth disease type 2B2
Inborn genetic diseases
Other Variants in PNKP
rs267606956 rs587784365 rs267606957 rs374745816 rs200611702 rs376854895 rs116192442 rs148491228 rs201503405 rs144284975
Ask Dr. Hemsworth about this variant