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.
Asthma
CUI: C0004096
Disease: Asthma
1536 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.100 1.000 16 2004 2018
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.090 1.000 9 2010 2017
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.080 1.000 8 2001 2019
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.080 1.000 8 2002 2013
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.080 1.000 8 2001 2019
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.070 1.000 7 2001 2013
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.060 1.000 6 2009 2018
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.050 1.000 5 2004 2013
melanoma
CUI: C0025202
Disease: melanoma
515 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.050 1.000 5 2009 2016
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.050 1.000 5 2004 2019
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2008 2016
Anemia
CUI: C0002871
Disease: Anemia
94 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2009 2018
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
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2011 2014
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2008 2018
Epithelial ovarian cancer
CUI: C0677886
Disease: Epithelial ovarian cancer
129 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2009 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2010 2018
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2010 2018
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2010 2018
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2010 2016
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2010 2018
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 1.000 3 2018 2019
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 Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2008 2016
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2010 2018