RS111671429 FBN1
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What This Variant Does
"CLNSIG=255
Associated Conditions
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Marfan syndrome
Geleophysic dysplasia
Weill-Marchesani syndrome
Familial thoracic aortic aneurysm and aortic dissection
Stiff skin syndrome
Ectopia lentis 1
isolated
autosomal dominant
Acromicric dysplasia
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Marfan syndrome
Geleophysic dysplasia
Other Variants in FBN1