RS147358856 PCNT
Upload your DNA to see your genotype for this variant.
Associated Conditions
PCNT-related disorder
Microcephalic osteodysplastic primordial dwarfism type II
Inborn genetic diseases
PCNT-related disorder
Microcephalic osteodysplastic primordial dwarfism type II
Inborn genetic diseases
Other Variants in PCNT