RS769251450 FBN1
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Associated Conditions
Stiff skin syndrome
Geleophysic dysplasia
Ectopia lentis 1
isolated
autosomal dominant
Weill-Marchesani syndrome
Marfan syndrome
Familial thoracic aortic aneurysm and aortic dissection
Acromicric dysplasia
Stiff skin syndrome
Geleophysic dysplasia
Ectopia lentis 1
isolated
autosomal dominant
Weill-Marchesani syndrome
Other Variants in FBN1