RS886037825 BGN

Health Risk Chr X:153504869
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Familial thoracic aortic aneurysm and aortic dissection
Meester-Loeys syndrome
X-linked spondyloepimetaphyseal dysplasia
Cardiovascular phenotype
Familial thoracic aortic aneurysm and aortic dissection
Meester-Loeys syndrome
X-linked spondyloepimetaphyseal dysplasia
Cardiovascular phenotype
Other Variants in BGN
rs2521213722 rs782136399 rs1556992691 rs782199865 rs782473084 rs138787321 rs1166225684 rs2124232156 rs782449715 rs2521219168
Ask Dr. Hemsworth about this variant