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.
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
49 0.821 0.071 11 1219991 regulatory region variant G/A,T snp 2.6E-04; 7.7E-02 1.000 1.000 21 2011 2018
Hamman-Rich syndrome
CUI: C0085786
Disease: Hamman-Rich syndrome
9 0.821 0.071 11 1219991 regulatory region variant G/A,T snp 2.6E-04; 7.7E-02 0.050 1.000 5 2011 2017
Lung Diseases, Interstitial
CUI: C0206062
Disease: Lung Diseases, Interstitial
121 0.821 0.071 11 1219991 regulatory region variant G/A,T snp 2.6E-04; 7.7E-02 0.030 1.000 3 2014 2015
Pneumonia, Interstitial
CUI: C0206061
Disease: Pneumonia, Interstitial
3 0.821 0.071 11 1219991 regulatory region variant G/A,T snp 2.6E-04; 7.7E-02 0.030 1.000 3 2011 2016
Connective Tissue Diseases
CUI: C0009782
Disease: Connective Tissue Diseases
6 0.821 0.071 11 1219991 regulatory region variant G/A,T snp 2.6E-04; 7.7E-02 0.020 1.000 2 2016 2016
Pulmonary Fibrosis
CUI: C0034069
Disease: Pulmonary Fibrosis
13 0.821 0.071 11 1219991 regulatory region variant G/A,T snp 2.6E-04; 7.7E-02 0.020 1.000 2 2013 2013
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
149 0.821 0.071 11 1219991 regulatory region variant G/A,T snp 2.6E-04; 7.7E-02 0.010 1 2014 2014