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
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
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2013 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2013 2013
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2008 2008
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
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
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
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
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