rs17757541, BCL2

N. diseases: 7
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.
B-Cell Lymphomas
CUI: C0079731
Disease: B-Cell Lymphomas
42 0.827 0.240 18 63212453 intron variant C/G;T snv 0.020 1.000 2 2013 2015
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.827 0.240 18 63212453 intron variant C/G;T snv 0.010 1.000 1 2013 2013
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.827 0.240 18 63212453 intron variant C/G;T snv 0.010 1.000 1 2011 2011
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.827 0.240 18 63212453 intron variant C/G;T snv 0.010 1.000 1 2015 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.240 18 63212453 intron variant C/G;T snv 0.010 1.000 1 2015 2015
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.240 18 63212453 intron variant C/G;T snv 0.010 1.000 1 2015 2015
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.827 0.240 18 63212453 intron variant C/G;T snv 0.010 1.000 1 2016 2016