RS574183358 PIGT
Upload your DNA to see your genotype for this variant.
Associated Conditions
Multiple congenital anomalies-hypotonia-seizures syndrome 3
Paroxysmal nocturnal hemoglobinuria 2
Multiple congenital anomalies-hypotonia-seizures syndrome 3
Paroxysmal nocturnal hemoglobinuria 2
Other Variants in PIGT