RS368726848 FBN1
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Associated Conditions
Ectopia lentis 1
isolated
autosomal dominant
Marfan syndrome
Stiff skin syndrome
Acromicric dysplasia
Familial thoracic aortic aneurysm and aortic dissection
Geleophysic dysplasia
Weill-Marchesani syndrome
Ectopia lentis 1
isolated
autosomal dominant
Marfan syndrome
Stiff skin syndrome
Acromicric dysplasia
Other Variants in FBN1