Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0264490
Disease: Acute respiratory failure
Acute respiratory failure
0.010 1.000 1 2012 2012
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
0.020 1.000 2 2007 2016
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.010 1.000 1 2014 2014
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0.010 1.000 1 2007 2007
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
0.010 1.000 1 2017 2017
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
0.050 1.000 5 2012 2018
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 1.000 2 2014 2016
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2014 2014
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0007140
Disease: Carcinosarcoma
Carcinosarcoma
0.010 1.000 1 2010 2010
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
Childhood Embryonal Rhabdomyosarcoma
0.010 1.000 1 2018 2018
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma
0.010 1.000 1 2017 2017
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C1511789
Disease: Desmoplastic
Desmoplastic
0.010 1.000 1 2013 2013
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0206656
Disease: Embryonal Rhabdomyosarcoma
Embryonal Rhabdomyosarcoma
0.010 1.000 1 2018 2018
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.010 1.000 1 2017 2017
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 1.000 1 2017 2017
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2017 2017
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes
0.010 1.000 1 2005 2005
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute
0.010 1.000 1 2012 2012
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.010 1.000 1 2013 2013
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms
0.020 1.000 2 2014 2016
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2014 2014
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C4551686
Disease: Malignant neoplasm of soft tissue
Malignant neoplasm of soft tissue
0.010 1.000 1 2011 2011
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs1444669684
rs1444669684
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.020 1.000 2 2002 2006