RS587776739 AP1S2

Health Risk Chr X:15845898
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Pettigrew syndrome
Pettigrew syndrome
Other Variants in AP1S2
rs2519915767 rs1933972061 rs1934209113 rs2519929746 rs1934205000 rs2519929717 rs2519914292 rs2519914351 rs2519929432 rs1934288587
Ask Dr. Hemsworth about this variant