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: rs11016883
rs11016883
10 129702676 intron variant G/C snv 0.38
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2013 2013
dbSNP: rs3750824
rs3750824
10 129759310 missense variant G/A snv 8.5E-04 2.9E-04
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs3750824
rs3750824
10 129759310 missense variant G/A snv 8.5E-04 2.9E-04
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs4751108
rs4751108
10 129642165 intron variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs477692
rs477692
10 129627758 intron variant T/C snv 0.45
CUI: C3546688
Disease: response to temozolomide
response to temozolomide
0.700 1.000 1 2012 2012
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.070 1.000 7 2005 2018
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.070 1.000 7 2005 2018
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.040 1.000 4 2009 2018
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.030 1.000 3 2013 2019
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.030 1.000 3 2013 2019
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.030 1.000 3 2006 2014
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.030 1.000 3 2013 2019
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
Malignant neoplasm of colon and/or rectum
0.030 1.000 3 2006 2014
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2012 2014
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.020 1.000 2 2005 2019
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 2007 2010
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
Neoplasms 0.020 1.000 2 2005 2018
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm
Neoplasms 0.020 1.000 2 2005 2018
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2017 2019
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.020 1.000 2 2005 2019
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
Neoplasms; Stomatognathic Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
Familial multiple trichoepitheliomata
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2006 2006
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs12917
rs12917
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14
Malignant neoplasm of urinary bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2005 2005