RS146726731 FBN1
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What This Variant Does
"CLNSIG=255
Associated Conditions
Marfan syndrome
Acromicric dysplasia
Ectopia lentis 1
isolated
autosomal dominant
Geleophysic dysplasia
Weill-Marchesani syndrome
Familial thoracic aortic aneurysm and aortic dissection
Stiff skin syndrome
Connective tissue disorder
Lipodystrophy - childhood onset
Marfan syndrome
Acromicric dysplasia
Ectopia lentis 1
isolated
Other Variants in FBN1