RS758705082 PCNT

Health Risk Chr 21:46416376
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Associated Conditions
Inborn genetic diseases
PCNT-related disorder
Microcephalic osteodysplastic primordial dwarfism type II
Inborn genetic diseases
PCNT-related disorder
Microcephalic osteodysplastic primordial dwarfism type II
Other Variants in PCNT
rs119479061 rs397509366 rs397514033 rs119479062 rs1601795448 rs119479063 rs119479064 rs1569239749 rs2148093442 rs387906928
Ask Dr. Hemsworth about this variant