RS145105768 FBN1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Familial thoracic aortic aneurysm and aortic dissection
Weill-Marchesani syndrome
Acromicric dysplasia
Geleophysic dysplasia
Marfan syndrome
Ectopia lentis 1
isolated
autosomal dominant
Stiff skin syndrome
Familial thoracic aortic aneurysm and aortic dissection
Weill-Marchesani syndrome
Acromicric dysplasia
Geleophysic dysplasia
Marfan syndrome
Ectopia lentis 1
Other Variants in FBN1