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.
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