RS1060499763 PIGN
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Abnormal brain morphology
Multiple congenital anomalies-hypotonia-seizures syndrome 1
PIGN-related disorder
Abnormal brain morphology
Multiple congenital anomalies-hypotonia-seizures syndrome 1
PIGN-related disorder
Other Variants in PIGN