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: rs398122859
rs398122859
1.000 0.120 12 112453210 frameshift variant CT/- delins
CUI: C0410530
Disease: Metachondromatosis
Metachondromatosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases 0.700 0
dbSNP: rs398122860
rs398122860
1.000 0.120 12 112486564 frameshift variant C/- delins
CUI: C0410530
Disease: Metachondromatosis
Metachondromatosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases 0.700 0
dbSNP: rs398122861
rs398122861
1.000 0.120 12 112455948 splice acceptor variant A/C snv
CUI: C0410530
Disease: Metachondromatosis
Metachondromatosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases 0.700 0
dbSNP: rs398122862
rs398122862
1.000 0.120 12 112482073 splice acceptor variant G/T snv
CUI: C0410530
Disease: Metachondromatosis
Metachondromatosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases 0.700 0