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.
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
Xeroderma Pigmentosum, Complementation Group D
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
111 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2011 2011
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
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
Vomiting
CUI: C0042963
Disease: Vomiting
23 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2019 2019
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2011 2011
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2012 2012
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
Testicular Germ Cell Tumor
CUI: C1336708
Disease: Testicular Germ Cell Tumor
93 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
TARSAL-CARPAL COALITION SYNDROME
CUI: C1861305
Disease: TARSAL-CARPAL COALITION SYNDROME
13 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2019 2019
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
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2013 2013
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
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.030 0.333 3 2007 2013
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2019 2019
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
Small cell carcinoma of lung
CUI: C0149925
Disease: Small cell carcinoma of lung
125 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2012 2012
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
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2012 2012
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
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT
CUI: C2678061
Disease: SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT
12 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2010 2010
Rhinitis
CUI: C0035455
Disease: Rhinitis
20 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2018 2018
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2008 2008
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