RS201273753 FBN1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Acute aortic dissection
Congenital aneurysm of ascending aorta
8 conditions
Stiff skin syndrome
Geleophysic dysplasia
Acromicric dysplasia
Ectopia lentis 1
isolated
autosomal dominant
Weill-Marchesani syndrome
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Marfan syndrome
Other Variants in FBN1