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: rs587777450
rs587777450
0.790 0.320 18 10671729 missense variant C/T snv
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases 0.800 1.000 1 2014 2014