RS773624614 PIGT

Health Risk Chr 20:45420609
Upload your DNA to see your genotype for this variant.
Associated Conditions
Multiple congenital anomalies-hypotonia-seizures syndrome 3
Paroxysmal nocturnal hemoglobinuria 2
Inborn genetic diseases
Multiple congenital anomalies-hypotonia-seizures syndrome 3
Paroxysmal nocturnal hemoglobinuria 2
Inborn genetic diseases
Other Variants in PIGT
rs587777027 rs587777028 rs527236031 rs527236032 rs756632799 rs139366969 rs201317502 rs149740779 rs574183358 rs771691280
Ask Dr. Hemsworth about this variant