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.
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2015 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2011 2016
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2016 2016
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2013 2017
Asthma
CUI: C0004096
Disease: Asthma
1536 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.090 0.889 9 2007 2018
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2018 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2019 2019
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