RS151020551 PCNT

Health Risk Chr 21:46363699
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Microcephalic osteodysplastic primordial dwarfism type II
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