rs1800925, IL13;TH2LCRR

N. diseases: 37
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.
Schistosoma hematobium infection
CUI: C0276926
Disease: Schistosoma hematobium infection
3 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2012 2012
Appendicitis
CUI: C0003615
Disease: Appendicitis
10 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2020 2020
Rhinoconjunctivitis
CUI: C0861155
Disease: Rhinoconjunctivitis
16 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2011 2011
Rhinitis
CUI: C0035455
Disease: Rhinitis
20 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2008 2010
Complicated malaria
CUI: C2747816
Disease: Complicated malaria
38 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2009 2009
Hay fever
CUI: C0018621
Disease: Hay fever
42 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2011 2011
Wheezing
CUI: C0043144
Disease: Wheezing
54 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2013 2013
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
63 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2013 2013
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2015 2015
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2011 2011
Psoriasis vulgaris
CUI: C0263361
Disease: Psoriasis vulgaris
80 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2011 2011
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
89 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.030 1.000 3 2009 2011
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2007 2007
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2007 2007
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2016 2016
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2016 2016
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2015 2015
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.050 0.400 5 2008 2018
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2007 2007
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2013 2013
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2013 2013
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2013 2013
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2007 2007
Glioma
CUI: C0017638
Disease: Glioma
353 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2013 2015
Eczema
CUI: C0013595
Disease: Eczema
368 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.020 0.500 2 2011 2011