rs1695, GSTP1

N. diseases: 100
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.
Childhood Medulloblastoma
CUI: C0278510
Disease: Childhood Medulloblastoma
1 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2013 2013
HODGKIN'S AND NON-HODGKIN'S LYMPHOMA
2 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2013 2013
Leukoplakia, Oral
CUI: C0023532
Disease: Leukoplakia, Oral
2 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2011 2011
Malignant neoplasm of brain
CUI: C0153633
Disease: Malignant neoplasm of brain
3 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
Thickening of pleura
CUI: C0264545
Disease: Thickening of pleura
4 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2007 2007
Cleft Lip with or without Cleft Palate
6 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2008 2008
Cutaneous Mastocytosis
CUI: C1136033
Disease: Cutaneous Mastocytosis
6 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2017 2017
Maternal hypertension
CUI: C0565599
Disease: Maternal hypertension
6 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2004 2004
Aplasia Cutis Congenita
CUI: C0282160
Disease: Aplasia Cutis Congenita
7 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2009 2009
Chronic Kidney Insufficiency
CUI: C0403447
Disease: Chronic Kidney Insufficiency
7 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2009 2009
Acoustic Neuroma
CUI: C0027859
Disease: Acoustic Neuroma
8 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2003 2003
Bronchial Hyperreactivity
CUI: C0085129
Disease: Bronchial Hyperreactivity
9 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.020 1.000 2 2008 2013
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
14 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2003 2003
Vomiting
CUI: C0042963
Disease: Vomiting
14 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2018 2018
Polyp of large intestine
CUI: C0949059
Disease: Polyp of large intestine
15 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1 2006 2006
Lung diseases
CUI: C0024115
Disease: Lung diseases
18 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2004 2004
Xeroderma pigmentosum, group F
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
19 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.020 1.000 2 2013 2017
Agenesis of corpus callosum
CUI: C0175754
Disease: Agenesis of corpus callosum
19 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2009 2009
Drug abuse
CUI: C0013146
Disease: Drug abuse
25 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2005 2005
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
26 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.020 1.000 2 2013 2017
Rash and Dermatitis Adverse Event Associated with Chemoradiation
27 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2016 2016
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
30 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2014 2014
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
31 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.020 1.000 2 2007 2010
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
33 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2006 2006
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
34 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 0.010 1.000 1 2018 2018