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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2003 2011
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2006 2010
Pseudohyperkalemia Cardiff
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
60 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2005 2012
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2000 2004
Serum iron measurement
CUI: C1318312
Disease: Serum iron measurement
25 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.700 1.000 2 2011 2017
Thalassemia
CUI: C0039730
Disease: Thalassemia
18 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2007 2007
Thalassemia trait
CUI: C0702157
Disease: Thalassemia trait
2 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.020 1.000 2 2005 2017
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