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Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBN2
(N2662S)
Single nucleotide variant
(missense variant)
Congenital contractural arachnodactyly
+1 more
GConflicting classifications of pathogenicity
FBN2
(D2532N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FBN2
(R2329Q)
Single nucleotide variant
(missense variant)
Congenital contractural arachnodactyly
+2 more
GConflicting classifications of pathogenicity
FBN2
(I2316F)
Single nucleotide variant
(missense variant)
Connective tissue disorder
+5 more
GConflicting classifications of pathogenicity
FBN2
(N2240S)
Single nucleotide variant
(missense variant)
Congenital contractural arachnodactyly
+1 more
GConflicting classifications of pathogenicity
FBN2
(P2085S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FBN2
(D1588V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
FBN2
(S1420N)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
FBN2
(C1378*)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
FBN2
(G1251E)
Single nucleotide variant
(missense variant)
Congenital contractural arachnodactyly
+1 more
GUncertain significance
FBN2
Single nucleotide variant
(splice acceptor variant)
not provided
GUncertain significance
FBN2
(G1094R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FBN2
(R934Q)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
FBN2
(E846K)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
FBN2
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
FBN2
(C744fs)
Deletion
(frameshift variant)
not provided
GUncertain significance
FBN2
(K725N)
Single nucleotide variant
(missense variant)
Congenital contractural arachnodactyly
+1 more
GUncertain significance
FBN2
(T700I)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
FBN2
(L585P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FBN2
(D575H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FBN2
(R347C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FBN2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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