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 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
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
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
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
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
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
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