rs2308321, MGMT

N. diseases: 29
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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.040 1.000 4 2009 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.040 1.000 4 2009 2013
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.020 1.000 2 2006 2012
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.020 0.500 2 2010 2019
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.020 1.000 2 2006 2012
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.020 0.500 2 2010 2019
Albinism, Oculocutaneous
CUI: C0078918
Disease: Albinism, Oculocutaneous
45 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2017 2017
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2006 2006
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2013 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2006 2006
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1 2006 2006
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2013 2013
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2013 2013
Familial multiple trichoepitheliomata
32 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2008 2008
Glioma
CUI: C0017638
Disease: Glioma
353 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2007 2007
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2005 2005
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2017 2017
Lymphoma, Follicular
CUI: C0024301
Disease: Lymphoma, Follicular
83 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2014 2014
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2007 2007
Malignant Glioma
CUI: C0555198
Disease: Malignant Glioma
22 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2017 2017
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2005 2005
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2006 2006
Malignant neoplasm of colon and/or rectum
502 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2006 2006
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1 2006 2006
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 0.010 1.000 1 2013 2013