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.
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2013 2016
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2016 2020
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2010 2015
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2010 2015
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
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2013 2018
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2011 2013
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2009 2013
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 0.500 2 2017 2018
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2010 2015
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2011 2013
Metastatic Colorectal Carcinoma
CUI: C4744564
Disease: Metastatic Colorectal Carcinoma
7 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2007 2010
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2015 2015
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2008 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2007 2012
Neutropenia
CUI: C0027947
Disease: Neutropenia
97 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2013 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2003 2017
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
Wheezing
CUI: C0043144
Disease: Wheezing
54 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2008 2010
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
82 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2013 2016
Xeroderma pigmentosum, group F
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
31 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2013 2016
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
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2017 2017
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
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