rs7216389, GSDMB

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
1536 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.900 0.889 18 2007 2018
Allergic Reaction
CUI: C1527304
Disease: Allergic Reaction
1019 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.700 1.000 1 2013 2013
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.700 1.000 1 2012 2012
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.080 1.000 8 2008 2018
Wheezing
CUI: C0043144
Disease: Wheezing
54 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.030 0.667 3 2009 2015
Adult onset asthma
CUI: C0741260
Disease: Adult onset asthma
67 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2014 2014
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2013 2013
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2015 2015
Aspirin exacerbated respiratory disease
CUI: C3853540
Disease: Aspirin exacerbated respiratory disease
32 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2017 2017
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2015 2015
Bronchial Hyperreactivity
CUI: C0085129
Disease: Bronchial Hyperreactivity
18 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2012 2012
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2015 2015
Eczema
CUI: C0013595
Disease: Eczema
368 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2009 2009
Glioma
CUI: C0017638
Disease: Glioma
353 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2011 2011