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: rs137852983
rs137852983
1.000 0.280 2 144389740 missense variant T/C snv
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.800 1.000 5 2001 2011
dbSNP: rs1135401790
rs1135401790
1.000 0.280 2 144389926 missense variant C/T snv
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1135402759
rs1135402759
1.000 0.280 2 144389932 missense variant T/C snv
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553960788
rs1553960788
1.000 0.280 2 144389978 missense variant G/A snv
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553961332
rs1553961332
1.000 0.280 2 144396456 missense variant A/C snv
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs397515448
rs397515448
1.000 0.280 2 144389885 missense variant A/G snv
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs397515449
rs397515449
1.000 0.280 2 144389962 missense variant T/C snv
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs863224942
rs863224942
1.000 0.280 2 144396547 missense variant C/A snv
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs398124282
rs398124282
1.000 0.280 2 144517276 splice donor variant A/G snv
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 1.000 1 2005 2005
dbSNP: rs786204805
rs786204805
1.000 0.280 2 144400005 splice donor variant TGGTTCTGTTT/CATTAATTTTAAGTCA delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs786204813
rs786204813
1.000 0.280 2 144517277 splice donor variant C/- delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs727503784
rs727503784
1.000 0.280 2 144429811 frameshift variant A/- del
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 1.000 2 1991 2008
dbSNP: rs1060500653
rs1060500653
1.000 0.280 2 144390001 frameshift variant C/- del
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553961487
rs1553961487
1.000 0.280 2 144398381 frameshift variant C/- delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553961510
rs1553961510
1.000 0.280 2 144398498 frameshift variant -/T delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553961580
rs1553961580
1.000 0.280 2 144398960 frameshift variant A/- del
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553961585
rs1553961585
1.000 0.280 2 144398972 frameshift variant -/GGAG delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553961695
rs1553961695
1.000 0.280 2 144399645 frameshift variant -/T ins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553961747
rs1553961747
1.000 0.280 2 144400019 frameshift variant T/- delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553962198
rs1553962198
1.000 0.280 2 144404947 frameshift variant C/- del
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553964145
rs1553964145
1.000 0.280 2 144429852 frameshift variant -/C delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553964147
rs1553964147
1.000 0.280 2 144429865 frameshift variant CA/- delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1553971826
rs1553971826
1.000 0.280 2 144517279 frameshift variant -/T delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1560605892
rs1560605892
1.000 0.280 2 144398430 frameshift variant C/- delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs1560606294
rs1560606294
1.000 0.280 2 144398850 frameshift variant C/- delins
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0