GSTM1, glutathione S-transferase mu 1, 2944

N. diseases: 627; N. variants: 9
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: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.020 1.000 2 2001 2013
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
Malignant neoplasm of urinary bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.020 1.000 2 2001 2013
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.020 1.000 2 2001 2013
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.040 0.750 4 2003 2017
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.040 0.750 4 2003 2017
dbSNP: rs1192077068
rs1192077068
1.000 0.160 1 109687896 stop gained G/A snv 1.5E-05
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.010 1.000 1 2005 2005
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
Digestive System Diseases; Neoplasms 0.010 1.000 1 2005 2005
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0949059
Disease: Polyp of large intestine
Polyp of large intestine
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Neoplasms 0.010 1.000 1 2005 2005
dbSNP: rs753904217
rs753904217
1.000 0.080 1 109690557 missense variant G/A snv 1.9E-04 6.6E-05
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2006 2006
dbSNP: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2008 2017
dbSNP: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2008 2017
dbSNP: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2008 2017
dbSNP: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
CUI: C0003949
Disease: Asbestosis
Asbestosis
Respiratory Tract Diseases; Occupational Diseases 0.010 1.000 1 2008 2008
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
0.010 1.000 1 2008 2008
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2008 2008
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
Childhood Acute Lymphoblastic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1065411
rs1065411
0.925 0.080 1 109690516 missense variant G/A;C;T snv 0.36; 6.9E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs1065411
rs1065411
0.925 0.080 1 109690516 missense variant G/A;C;T snv 0.36; 6.9E-06
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2010 2010
dbSNP: rs1344469579
rs1344469579
1 109688179 missense variant G/A snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 < 0.001 1 2010 2010
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 < 0.001 1 2010 2010
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2012 2014