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.
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
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
Bronchial Hyperreactivity
CUI: C0085129
Disease: Bronchial Hyperreactivity
18 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2005 2013
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2005 2012
Adult Hodgkin Lymphoma
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
27 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2005 2012
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2005 2016
Childhood Hodgkin Lymphoma
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
29 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2005 2012
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2005 2012
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
Neuropathy
CUI: C0442874
Disease: Neuropathy
110 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.040 0.500 4 2006 2013
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.100 0.818 11 2007 2019