RS1029955995 PCNT

Health Risk Chr 21:46385832
Upload your DNA to see your genotype for this variant.
Associated Conditions
PCNT-related disorder
Inborn genetic diseases
PCNT-related disorder
Inborn genetic diseases
Other Variants in PCNT
rs119479061 rs397509366 rs397514033 rs119479062 rs1601795448 rs119479063 rs119479064 rs1569239749 rs2148093442 rs387906928
Ask Dr. Hemsworth about this variant