Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C1527249
Disease: Colorectal Cancer
Colorectal Cancer
0.100 0.824 17 2002 2018
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.100 0.882 17 2002 2016
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.813 16 2002 2018
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.100 0.786 14 2004 2015
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.100 0.786 14 2004 2015
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 0.769 13 2006 2018
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 1.000 11 2002 2018
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
Childhood Acute Lymphoblastic Leukemia
0.100 0.700 10 2007 2016
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.090 0.889 9 2001 2007
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.090 1.000 9 2004 2018
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.080 0.875 8 2005 2015
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
0.080 0.875 8 2001 2008
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects
0.070 0.857 7 1999 2016
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
Diabetes Mellitus, Non-Insulin-Dependent
0.060 1.000 6 2000 2018
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.060 1.000 6 2003 2006
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.060 1.000 6 2000 2012
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.060 0.667 6 2003 2016
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.060 0.833 6 2002 2011
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.060 1.000 6 2003 2015
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.050 1.000 5 2004 2012
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.050 0.800 5 2008 2016
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.050 0.800 5 2004 2014
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.050 0.800 5 2008 2016
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.050 1.000 5 2004 2012
dbSNP: rs397507444
rs397507444
0.457 0.714 1 11794407 missense variant T/G snp
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.050 0.800 5 2004 2014