rs1695, GSTP1

N. diseases: 100
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.
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
96 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2002 2002
Acoustic Neuroma
CUI: C0027859
Disease: Acoustic Neuroma
8 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2003 2003
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
14 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2003 2003
Lung diseases
CUI: C0024115
Disease: Lung diseases
18 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2004 2004
Maternal hypertension
CUI: C0565599
Disease: Maternal hypertension
6 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2004 2004
Sporadic Breast Carcinoma
CUI: C1336076
Disease: Sporadic Breast Carcinoma
37 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2004 2004
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
48 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Drug abuse
CUI: C0013146
Disease: Drug abuse
25 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
145 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
36 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
71 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Malignant neoplasm of brain
CUI: C0153633
Disease: Malignant neoplasm of brain
3 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
106 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Nonorganic psychosis
CUI: C0349204
Disease: Nonorganic psychosis
60 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Psychotic Disorders
CUI: C0033975
Disease: Psychotic Disorders
113 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Uterine Corpus Cancer
CUI: C1883486
Disease: Uterine Corpus Cancer
106 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Allergic disposition
CUI: C3539909
Disease: Allergic disposition
37 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.020 1.000 2 2004 2006
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
33 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2006 2006
Polyp of large intestine
CUI: C0949059
Disease: Polyp of large intestine
15 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1 2006 2006
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
674 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1 2007 2007
Lymphoma, Follicular
CUI: C0024301
Disease: Lymphoma, Follicular
74 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2007 2007
Thickening of pleura
CUI: C0264545
Disease: Thickening of pleura
4 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2007 2007
Adenoma
CUI: C0001430
Disease: Adenoma
73 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2008 2008
Cleft Lip with or without Cleft Palate
6 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2008 2008
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
784 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2008 2008