RS267606798 FBN1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Stiff skin syndrome
Marfan syndrome
Weill-Marchesani syndrome 2
dominant
Stiff skin syndrome
Marfan syndrome
Weill-Marchesani syndrome 2
dominant
Other Variants in FBN1