RS750036723 FBN1
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Associated Conditions
Weill-Marchesani syndrome
Stiff skin syndrome
Familial thoracic aortic aneurysm and aortic dissection
Ectopia lentis 1
isolated
autosomal dominant
Acromicric dysplasia
Marfan syndrome
Geleophysic dysplasia
Weill-Marchesani syndrome
Stiff skin syndrome
Familial thoracic aortic aneurysm and aortic dissection
Ectopia lentis 1
isolated
autosomal dominant
Other Variants in FBN1