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.
Anemia
CUI: C0002871
Disease: Anemia
94 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1 2017 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2017 2017
Autoimmune thrombocytopenia
CUI: C0242584
Disease: Autoimmune thrombocytopenia
7 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2016 2016
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2012 2012
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2015 2015
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2009 2009
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2016 2016
Gastrointestinal Neoplasms
CUI: C0017185
Disease: Gastrointestinal Neoplasms
3 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2019 2019
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2013 2013
Immune Reconstitution Inflammatory Syndrome
CUI: C1619738
Disease: Immune Reconstitution Inflammatory Syndrome
5 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2014 2014
Immune reconstitution inflammatory syndrome [IRIS]
CUI: C2976853
Disease: Immune reconstitution inflammatory syndrome [IRIS]
1 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2014 2014
Intervertebral disc disorder
CUI: C0158252
Disease: Intervertebral disc disorder
19 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2016 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2013 2013
Malaria, Falciparum
CUI: C0024535
Disease: Malaria, Falciparum
19 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2017 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2015 2015
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2010 2010
Mitral Valve Stenosis
CUI: C0026269
Disease: Mitral Valve Stenosis
7 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2018 2018
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2008 2008
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2014 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2010 2010
Thrombocytopenia due to platelet alloimmunization
CUI: C0272286
Disease: Thrombocytopenia due to platelet alloimmunization
7 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2016 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2013 2013
Uveomeningoencephalitic Syndrome
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
27 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.010 1.000 1 2016 2016