RS781050795 ACP5

Health Risk Chr 19:11576780
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Spondyloenchondrodysplasia with immune dysregulation
Inborn genetic diseases
ACP5-related disorder
Spondyloenchondrodysplasia with immune dysregulation
Inborn genetic diseases
ACP5-related disorder
Other Variants in ACP5
rs387906668 rs387906669 rs387906670 rs781199182 rs139822120 rs147025508 rs369804864 rs879255600 rs878853218 rs1025967277
Ask Dr. Hemsworth about this variant