RS560004254 FBN1

Health Risk Chr 15:48644945
Upload your DNA to see your genotype for this variant.
Associated Conditions
Acromicric dysplasia
Geleophysic dysplasia
Ectopia lentis 1
isolated
autosomal dominant
Familial thoracic aortic aneurysm and aortic dissection
Marfan syndrome
Weill-Marchesani syndrome
Stiff skin syndrome
Acromicric dysplasia
Geleophysic dysplasia
Ectopia lentis 1
isolated
autosomal dominant
Familial thoracic aortic aneurysm and aortic dissection
Other Variants in FBN1
rs137854456 rs137854457 rs267606796 rs137854458 rs137854459 rs137854460 rs137854470 rs137854471 rs267606797 rs137854461
Ask Dr. Hemsworth about this variant