MGMT, O-6-methylguanine-DNA methyltransferase, 4255

N. diseases: 444; N. variants: 24
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2308327
rs2308327
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2308327
rs2308327
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs2308327
rs2308327
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2308327
rs2308327
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs2308327
rs2308327
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02
Xeroderma Pigmentosum, Complementation Group D
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.010 1.000 1 2006 2006
dbSNP: rs2308327
rs2308327
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME
Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2308327
rs2308327
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02
Familial multiple trichoepitheliomata
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs2308327
rs2308327
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2308327
rs2308327
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2007 2007
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.040 1.000 4 2009 2013
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.040 1.000 4 2009 2013
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.020 0.500 2 2010 2019
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.020 1.000 2 2006 2012
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.020 1.000 2 2006 2012
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.020 0.500 2 2010 2019
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME
Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
Neoplasms 0.010 1.000 1 2005 2005
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2007 2007
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2006 2006
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2006 2006
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2308321
rs2308321
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2006 2006