Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
50 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2005 2006
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1 2007 2007
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
Adrenoleukodystrophy
CUI: C0162309
Disease: Adrenoleukodystrophy
116 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2007 2010
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2005 2006
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2015 2015
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2004 2004
Adult Solid Neoplasm
CUI: C0280099
Disease: Adult Solid Neoplasm
3 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2015 2015
Alcoholic Liver Diseases
CUI: C0023896
Disease: Alcoholic Liver Diseases
20 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 1999 2001
alpha 1-Antitrypsin Deficiency
CUI: C0221757
Disease: alpha 1-Antitrypsin Deficiency
48 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2010 2017
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.800 0.882 17 2003 2016
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.100 0.636 11 2007 2016
Amyotrophic Lateral Sclerosis, Sporadic
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
90 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.030 0.667 3 2011 2014
Anemia
CUI: C0002871
Disease: Anemia
94 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1 2005 2005
Anemia, Pernicious
CUI: C0002892
Disease: Anemia, Pernicious
4 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2008 2008
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2003 2003
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2010 2010
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.040 1.000 4 1998 2019
Arthralgia
CUI: C0003862
Disease: Arthralgia
27 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2007 2007
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1 2006 2006
Arthropathy
CUI: C0022408
Disease: Arthropathy
10 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2006 2008
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.040 1.000 4 1998 2019
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2011 2011
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1 2008 2008