RS150882711 PCNT

Health Risk Chr 21:46427633
Upload your DNA to see your genotype for this variant.
Associated Conditions
Microcephalic osteodysplastic primordial dwarfism type II
PCNT-related disorder
Microcephalic osteodysplastic primordial dwarfism type II
PCNT-related disorder
Other Variants in PCNT
rs119479061 rs397509366 rs397514033 rs119479062 rs1601795448 rs119479063 rs119479064 rs1569239749 rs2148093442 rs387906928
Ask Dr. Hemsworth about this variant