RS61746008 FBN1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Acromicric dysplasia
Weill-Marchesani syndrome
Geleophysic dysplasia
Ectopia lentis 1
isolated
autosomal dominant
Stiff skin syndrome
8 conditions
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Acromicric dysplasia
Weill-Marchesani syndrome
Geleophysic dysplasia
Other Variants in FBN1