rs1800477, BCL2

N. diseases: 12
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 carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.020 1.000 2 2007 2012
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.020 1.000 2 2007 2012
Fetal Alcohol Syndrome
CUI: C0015923
Disease: Fetal Alcohol Syndrome
8 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.020 1.000 2 2007 2007
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.020 1.000 2 2007 2012
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.010 1.000 1 2010 2010
B-Cell Lymphomas
CUI: C0079731
Disease: B-Cell Lymphomas
42 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.010 1.000 1 2012 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.010 1.000 1 2017 2017
Diabetes Mellitus, Insulin-Dependent
954 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.010 1 2001 2001
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.010 1.000 1 2011 2011
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.010 1.000 1 2014 2014
Secondary malignant neoplasm of lymph node
188 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.010 1.000 1 2017 2017
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
42 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 0.010 1.000 1 2011 2011