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.
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
99 0.457 0.714 1 11794407 missense variant T/G snp 0.100 0.882 17 2002 2016
Colorectal Cancer
CUI: C1527249
Disease: Colorectal Cancer
955 0.457 0.714 1 11794407 missense variant T/G snp 0.100 0.824 17 2002 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
539 0.457 0.714 1 11794407 missense variant T/G snp 0.100 0.813 16 2002 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.457 0.714 1 11794407 missense variant T/G snp 0.100 0.786 14 2004 2015
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1365 0.457 0.714 1 11794407 missense variant T/G snp 0.100 0.786 14 2004 2015
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
1782 0.457 0.714 1 11794407 missense variant T/G snp 0.100 0.769 13 2006 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.457 0.714 1 11794407 missense variant T/G snp 0.100 1.000 11 2002 2018
Childhood Acute Lymphoblastic Leukemia
97 0.457 0.714 1 11794407 missense variant T/G snp 0.100 0.700 10 2007 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.457 0.714 1 11794407 missense variant T/G snp 0.090 0.889 9 2001 2007
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1878 0.457 0.714 1 11794407 missense variant T/G snp 0.090 1.000 9 2004 2018
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
13 0.457 0.714 1 11794407 missense variant T/G snp 0.080 0.875 8 2001 2008
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
447 0.457 0.714 1 11794407 missense variant T/G snp 0.080 0.875 8 2005 2015
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
49 0.457 0.714 1 11794407 missense variant T/G snp 0.070 0.857 7 1999 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
197 0.457 0.714 1 11794407 missense variant T/G snp 0.060 0.833 6 2002 2011
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
189 0.457 0.714 1 11794407 missense variant T/G snp 0.060 1.000 6 2003 2006
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.457 0.714 1 11794407 missense variant T/G snp 0.060 1.000 6 2000 2018
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
110 0.457 0.714 1 11794407 missense variant T/G snp 0.060 1.000 6 2000 2012
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
154 0.457 0.714 1 11794407 missense variant T/G snp 0.060 1.000 6 2003 2015
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
784 0.457 0.714 1 11794407 missense variant T/G snp 0.060 0.667 6 2003 2016
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
9 0.457 0.714 1 11794407 missense variant T/G snp 0.050 0.800 5 2002 2016
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
240 0.457 0.714 1 11794407 missense variant T/G snp 0.050 0.800 5 2004 2014
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
563 0.457 0.714 1 11794407 missense variant T/G snp 0.050 1.000 5 2004 2012
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
341 0.457 0.714 1 11794407 missense variant T/G snp 0.050 0.800 5 2008 2016
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
135 0.457 0.714 1 11794407 missense variant T/G snp 0.050 0.800 5 2004 2014
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
756 0.457 0.714 1 11794407 missense variant T/G snp 0.050 1.000 5 2004 2012