RS56102085 FBN1

Health Risk Chr 15:48508573
Upload your DNA to see your genotype for this variant.
Associated Conditions
Weill-Marchesani syndrome
Marfan syndrome
Stiff skin syndrome
Acromicric dysplasia
Geleophysic dysplasia
Ectopia lentis 1
isolated
autosomal dominant
Familial thoracic aortic aneurysm and aortic dissection
FBN1-related disorder
Weill-Marchesani syndrome
Marfan syndrome
Stiff skin syndrome
Acromicric dysplasia
Geleophysic dysplasia
Other Variants in FBN1
rs137854456 rs137854457 rs267606796 rs137854458 rs137854459 rs137854460 rs137854470 rs137854471 rs267606797 rs137854461
Ask Dr. Hemsworth about this variant