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.
Adult Myelodysplastic Syndrome
CUI: C3900098
Disease: Adult Myelodysplastic Syndrome
20 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2008 2008
Childhood Myelodysplastic Syndrome
CUI: C2347761
Disease: Childhood Myelodysplastic Syndrome
20 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2008 2008
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
Maternal hypertension
CUI: C0565599
Disease: Maternal hypertension
22 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2003 2003
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
Childhood Medulloblastoma
CUI: C0278510
Disease: Childhood Medulloblastoma
25 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2013 2013
Necrotizing enterocolitis in fetus OR newborn
26 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1 2016 2016
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
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
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
Hematuria
CUI: C0018965
Disease: Hematuria
31 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2015 2015
Malignant neoplasm of testis
CUI: C0153594
Disease: Malignant neoplasm of testis
31 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2019 2019
Familial multiple trichoepitheliomata
32 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
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
Malignant neoplasm of skin
CUI: C0007114
Disease: Malignant neoplasm of skin
38 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1 2015 2015
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
39 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2010 2010
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
Dyskinetic syndrome
CUI: C0013384
Disease: Dyskinetic syndrome
42 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2010 2010
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2016 2016
Pregnancy associated hypertension
CUI: C0852036
Disease: Pregnancy associated hypertension
43 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2003 2003
Agenesis of corpus callosum
CUI: C0175754
Disease: Agenesis of corpus callosum
45 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
Hemochromatosis
CUI: C0018995
Disease: Hemochromatosis
45 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2015 2015
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
Carpal Tunnel Syndrome
CUI: C0007286
Disease: Carpal Tunnel Syndrome
46 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2016 2016
Pelvic Organ Prolapse
CUI: C0877015
Disease: Pelvic Organ Prolapse
49 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2014 2014