ADAM33, ADAM metallopeptidase domain 33, 80332

N. diseases: 49; N. variants: 22
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs44707
rs44707 		0.925 0.080 20 3670579 non coding transcript exon variant G/C;T snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs511898
rs511898 		0.925 0.080 20 3674438 3 prime UTR variant C/T snv 0.47
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs512625
rs512625 		0.925 0.120 20 3667731 upstream gene variant A/G;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.010 < 0.001 1 2008 2008
dbSNP: rs512625
rs512625 		0.925 0.120 20 3667731 upstream gene variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs528557
rs528557 		0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs528557
rs528557 		0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29
CUI: C0085129
Disease: Bronchial Hyperreactivity
Bronchial Hyperreactivity 		Respiratory Tract Diseases 0.010 1.000 1 2009 2009
dbSNP: rs528557
rs528557 		0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29
CUI: C0043144
Disease: Wheezing
Wheezing 		Pathological Conditions, Signs and Symptoms 0.010 < 0.001 1 2015 2015
dbSNP: rs528557
rs528557 		0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs574174
rs574174 		1.000 0.080 20 3670047 non coding transcript exon variant C/T snv 0.20
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs598418
rs598418 		1.000 0.080 20 3670622 non coding transcript exon variant G/A snv 0.63
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs612709
rs612709 		0.882 0.120 20 3671560 intron variant G/A snv 0.17 0.25
CUI: C0861155
Disease: Rhinoconjunctivitis
Rhinoconjunctivitis 		Eye Diseases 0.010 1.000 1 2012 2012
dbSNP: rs612709
rs612709 		0.882 0.120 20 3671560 intron variant G/A snv 0.17 0.25
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs612709
rs612709 		0.882 0.120 20 3671560 intron variant G/A snv 0.17 0.25
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs628977
rs628977 		0.851 0.160 20 3669074 intron variant T/C snv 0.65
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs628977
rs628977 		0.851 0.160 20 3669074 intron variant T/C snv 0.65
CUI: C0861155
Disease: Rhinoconjunctivitis
Rhinoconjunctivitis 		Eye Diseases 0.010 1.000 1 2012 2012
dbSNP: rs628977
rs628977 		0.851 0.160 20 3669074 intron variant T/C snv 0.65
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis 		Respiratory Tract Diseases 0.010 1.000 1 2014 2014
dbSNP: rs628977
rs628977 		0.851 0.160 20 3669074 intron variant T/C snv 0.65
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.010 < 0.001 1 2008 2008
dbSNP: rs677044
rs677044 		1.000 0.080 20 3668784 3 prime UTR variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs678881
rs678881 		0.925 0.080 20 3669156 intron variant G/A;C snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2787094
rs2787094 		0.851 0.160 20 3668514 3 prime UTR variant C/G snv 0.71
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 1.000 2 2013 2015
dbSNP: rs44707
rs44707 		0.925 0.080 20 3670579 non coding transcript exon variant G/C;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 1.000 2 2008 2013
dbSNP: rs511898
rs511898 		0.925 0.080 20 3674438 3 prime UTR variant C/T snv 0.47
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 1.000 2 2009 2018
dbSNP: rs528557
rs528557 		0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 0.500 2 2015 2017
dbSNP: rs678881
rs678881 		0.925 0.080 20 3669156 intron variant G/A;C snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 1.000 2 2013 2019
dbSNP: rs2280090
rs2280090 		0.882 0.120 20 3669558 missense variant G/A snv 0.13 0.14
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.030 1.000 3 2009 2019