rs5743618, TLR1

N. diseases: 14
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.
Asthma
CUI: C0004096
Disease: Asthma
729 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.710 1.000 2 2014 2017
Hypersensitivity
CUI: C0020517
Disease: Hypersensitivity
964 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.700 1 2017 2017
Leprosy
CUI: C0023343
Disease: Leprosy
148 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.020 1.000 2 2010 2013
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
124 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.020 1.000 2 2013 2015
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
22 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1.000 1 2014 2014
Candidemia
CUI: C0877445
Disease: Candidemia
9 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1.000 1 2012 2012
Cystic Fibrosis
CUI: C0010674
Disease: Cystic Fibrosis
489 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1.000 1 2014 2014
Dermatitis, Atopic
CUI: C0011615
Disease: Dermatitis, Atopic
173 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1.000 1 2014 2014
Gastric ulcer
CUI: C0038358
Disease: Gastric ulcer
7 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1.000 1 2013 2013
Ileal Diseases
CUI: C0020875
Disease: Ileal Diseases
6 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1 2006 2006
Malaria
CUI: C0024530
Disease: Malaria
107 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1.000 1 2008 2008
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
341 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1.000 1 2013 2013
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
364 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1.000 1 2013 2013
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
35 0.724 0.321 4 38797027 missense variant C/A snp 0.53 0.47 0.010 1.000 1 2011 2011