rs1695, GSTP1

N. diseases: 188
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
108 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2002 2002
Acoustic Neuroma
CUI: C0027859
Disease: Acoustic Neuroma
3 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2003 2003
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2003 2003
Maternal hypertension
CUI: C0565599
Disease: Maternal hypertension
22 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2003 2003
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2003 2003
Pregnancy associated hypertension
CUI: C0852036
Disease: Pregnancy associated hypertension
43 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2003 2003
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1 2004 2004
Lung diseases
CUI: C0024115
Disease: Lung diseases
50 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2004 2004
Ataxia Telangiectasia
CUI: C0004135
Disease: Ataxia Telangiectasia
698 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Drug abuse
CUI: C0013146
Disease: Drug abuse
39 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Drug-induced tardive dyskinesia
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
67 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Hypocalciuric hypercalcemia, familial, type 1
CUI: C0342637
Disease: Hypocalciuric hypercalcemia, familial, type 1
58 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Malignant neoplasm of brain
CUI: C0153633
Disease: Malignant neoplasm of brain
16 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Nonorganic psychosis
CUI: C0349204
Disease: Nonorganic psychosis
98 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Polyp of large intestine
CUI: C0949059
Disease: Polyp of large intestine
32 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Psychotic Disorders
CUI: C0033975
Disease: Psychotic Disorders
179 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Tardive Dyskinesia
CUI: C0686347
Disease: Tardive Dyskinesia
67 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Sporadic Breast Carcinoma
CUI: C1336076
Disease: Sporadic Breast Carcinoma
46 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2004 2006
Skin lesion
CUI: C0037284
Disease: Skin lesion
52 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2006 2006
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2007 2007
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1 2007 2007