rs2070600, AGER

N. diseases: 82
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.
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2002 2002
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2005 2005
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2005 2005
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.020 0.500 2 2005 2007
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.020 1.000 2 2010 2010
Pulmonary function
CUI: C0231921
Disease: Pulmonary function
259 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.700 1.000 2 2010 2010
Pulmonary function (finding)
CUI: C3160731
Disease: Pulmonary function (finding)
259 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.700 1.000 2 2010 2010
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2010 2010
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2010 2010
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2010 2010
Vascular inflammations
CUI: C0947751
Disease: Vascular inflammations
3 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2010 2010
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.710 1.000 3 2007 2011
Diabetes Mellitus, Insulin-Dependent
954 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.020 1.000 2 1999 2011
Respiratory Function Tests
CUI: C0035227
Disease: Respiratory Function Tests
108 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.700 1.000 3 2010 2012
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2012 2012
Intrahepatic Cholestasis
CUI: C0008372
Disease: Intrahepatic Cholestasis
3 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2012 2012
Psychoticism
CUI: C0687131
Disease: Psychoticism
2 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2012 2012
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2012 2012
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.030 0.333 3 2012 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2013 2013
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.020 0.500 2 2011 2014
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.020 1.000 2 2008 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.020 1.000 2 2008 2014
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.020 1.000 2 2008 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2014 2014