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.
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.020 1.000 2 2012 2019
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.020 1.000 2 2012 2019
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
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.030 1.000 3 2010 2016
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
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
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
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.020 1.000 2 2008 2013
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