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.
Lymphoma, Follicular
CUI: C0024301
Disease: Lymphoma, Follicular
83 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2007 2007
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
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 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
Cleft Lip with or without Cleft Palate
50 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2008 2008
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2008 2008
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
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
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
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
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
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
Chronic Kidney Insufficiency
CUI: C0403447
Disease: Chronic Kidney Insufficiency
12 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
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
Malaria
CUI: C0024530
Disease: Malaria
148 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
Peripheral Nervous System Diseases
CUI: C4721453
Disease: Peripheral Nervous System Diseases
69 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
81 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
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
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
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.020 1.000 2 2007 2010
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
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
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
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