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
1536 0.807 0.280 7 7968245 intron variant G/A;C snv 0.060 0.667 6 2015 2019
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.807 0.280 7 7968245 intron variant G/A;C snv 0.010 1.000 1 2017 2017
Craniosynostosis
CUI: C0010278
Disease: Craniosynostosis
90 0.807 0.280 7 7968245 intron variant G/A;C snv 0.010 1.000 1 2018 2018
Eosinophilia
CUI: C0014457
Disease: Eosinophilia
23 0.807 0.280 7 7968245 intron variant G/A;C snv 0.010 1.000 1 2014 2014
Eosinophilic disorder
CUI: C1306759
Disease: Eosinophilic disorder
22 0.807 0.280 7 7968245 intron variant G/A;C snv 0.010 1.000 1 2014 2014
Glucocorticoid Receptor Deficiency
CUI: C1841972
Disease: Glucocorticoid Receptor Deficiency
12 0.807 0.280 7 7968245 intron variant G/A;C snv 0.010 1.000 1 2018 2018
Hay fever
CUI: C0018621
Disease: Hay fever
42 0.807 0.280 7 7968245 intron variant G/A;C snv 0.010 1.000 1 2018 2018