RS112084407 FBN1
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What This Variant Does
"CLNSIG=255
Associated Conditions
Marfan syndrome
Ectopia lentis 1
isolated
autosomal dominant
Geleophysic dysplasia
Acromicric dysplasia
Connective tissue disorder
Familial thoracic aortic aneurysm and aortic dissection
FBN1-related disorder
Marfan syndrome
Ectopia lentis 1
isolated
autosomal dominant
Geleophysic dysplasia
Acromicric dysplasia
Other Variants in FBN1