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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBN2
(T2787S)
Single nucleotide variant
(missense variant)
Congenital contractural arachnodactyly
GUncertain significance
FBN2
(N1165K)
Single nucleotide variant
(missense variant)
Congenital contractural arachnodactyly
GUncertain significance
FBN2
(Y1146C)
Single nucleotide variant
(missense variant)
Congenital contractural arachnodactyly
GConflicting classifications of pathogenicity
FBN2
(A282T)
Single nucleotide variant
(missense variant)
Congenital contractural arachnodactyly
GUncertain significance
FBN2
Single nucleotide variant
(splice acceptor variant)
Congenital contractural arachnodactyly
GPathogenic
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