rs536289169, GSTM1;GSTM2

N. diseases: 13
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.
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.020 1.000 2 2008 2017
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.020 1.000 2 2012 2014
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.020 1.000 2 2008 2017
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.020 1.000 2 2008 2017
Asbestosis
CUI: C0003949
Disease: Asbestosis
2 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.010 1.000 1 2008 2008
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.010 1.000 1 2010 2010
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.010 1.000 1 2012 2012
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.010 1.000 1 2019 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.010 1.000 1 2019 2019
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.010 1.000 1 2014 2014
Intellectual Disability
CUI: C3714756
Disease: Intellectual Disability
159 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.010 1.000 1 2014 2014
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.010 1.000 1 2016 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 0.010 1.000 1 2012 2012