FBN2, fibrillin 2, 2201

N. diseases: 211; N. variants: 42
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs863223567
rs863223567
1.000 0.080 5 128338002 missense variant C/T snv
Congenital contractural arachnodactyly
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 0
dbSNP: rs869025428
rs869025428
1.000 0.080 5 128339061 missense variant T/A snv
Congenital contractural arachnodactyly
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 0
dbSNP: rs201988564
rs201988564
0.925 0.240 5 128464739 missense variant T/G snv 1.2E-05 2.1E-05
Congenital contractural arachnodactyly
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2002 2002