GSTM2, glutathione S-transferase mu 2, 2946

N. diseases: 195; N. variants: 11
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: 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: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.010 1.000 1 2014 2014
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: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.010 1.000 1 2014 2014
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
dbSNP: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs536289169
rs536289169
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04
CUI: C0014544
Disease: Epilepsy
Epilepsy
Nervous System Diseases 0.010 1.000 1 2014 2014
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: rs5776993
rs5776993
1.000 0.080 1 109680280 intron variant AAAAAAAA/-;AA;AAAA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA delins
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs638820
rs638820
0.827 0.160 1 109667284 intron variant G/A snv 0.52
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2010 2010
dbSNP: rs638820
rs638820
0.827 0.160 1 109667284 intron variant G/A snv 0.52
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2010 2010
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: rs768623239
rs768623239
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2014 2014
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: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
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: 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: 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