RS869312929 PCNT

Health Risk Chr 21:46388870
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Microcephalic osteodysplastic primordial dwarfism type II
Inborn genetic diseases
Microcephalic osteodysplastic primordial dwarfism type II
Other Variants in PCNT
rs119479061 rs397509366 rs397514033 rs119479062 rs1601795448 rs119479063 rs119479064 rs1569239749 rs2148093442 rs387906928
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