Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0004096
Disease: Asthma
Asthma 		0.900 0.889 14 2007 2018
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.080 1.000 8 2008 2018
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0043144
Disease: Wheezing
Wheezing 		0.030 0.667 3 2009 2015
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis 		0.010 1.000 1 2015 2015
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0013595
Disease: Eczema
Eczema 		0.010 1.000 1 2009 2009
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C3853540
Disease: Aspirin exacerbated respiratory disease
Aspirin exacerbated respiratory disease 		0.010 1.000 1 2017 2017
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2015 2015
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2011 2011
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2015 2015
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.010 1.000 1 2013 2013
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0085129
Disease: Bronchial Hyperreactivity
Bronchial Hyperreactivity 		0.010 1.000 1 2012 2012
dbSNP: rs7216389
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		0.010 1.000 1 2014 2014