RS397515802 FBN1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Stiff skin syndrome
Ectopia lentis 1
isolated
autosomal dominant
Geleophysic dysplasia 2
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Stiff skin syndrome
Ectopia lentis 1
isolated
autosomal dominant
Other Variants in FBN1