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
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
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
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
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
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
Brain Infarction
CUI: C0751955
Disease: Brain Infarction
11 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2001 2001
Calcium pyrophosphate deposition disease
CUI: C0553730
Disease: Calcium pyrophosphate deposition disease
5 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2007 2007
Carcinoma of Male Breast
CUI: C0238033
Disease: Carcinoma of Male Breast
38 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 1998 1998
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2008 2008
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2006 2006
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood 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
Childhood Solid Neoplasm
CUI: C0279068
Disease: Childhood 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
Chronic active hepatitis
CUI: C0520463
Disease: Chronic active hepatitis
34 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 1999 1999
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005