RS201361628 FBN1
Upload your DNA to see your genotype for this variant.
Associated Conditions
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Acromicric dysplasia
Ectopia lentis 1
isolated
autosomal dominant
Stiff skin syndrome
Weill-Marchesani syndrome
Cardiovascular phenotype
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Acromicric dysplasia
Ectopia lentis 1
isolated
autosomal dominant
Other Variants in FBN1