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.
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 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
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
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
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
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2013 2013
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
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2012 2012
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
Agranulocytosis
CUI: C0001824
Disease: Agranulocytosis
8 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2018 2018
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2018 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 0.500 2 2004 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
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2016 2016
Aplasia Cutis Congenita
CUI: C0282160
Disease: Aplasia Cutis Congenita
14 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
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
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
59 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2010 2010
Ataxia Telangiectasia
CUI: C0004135
Disease: Ataxia Telangiectasia
698 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2005 2005
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2016 2016
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
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