rs140693, MBD4

N. diseases: 10
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.
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 0.030 1.000 3 2006 2012
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 0.030 1.000 3 2006 2012
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 0.030 1.000 3 2006 2012
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 0.010 1.000 1 2006 2006
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 0.010 1.000 1 2012 2012
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 0.010 1.000 1 2012 2012
Malignant neoplasm of gastrointestinal tract
55 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 0.010 1.000 1 2009 2009
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 0.010 1.000 1 2012 2012
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 0.010 1 2012 2012
Squamous cell carcinoma of esophagus
329 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 0.010 1.000 1 2004 2004