Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7216389
rs7216389
0.900 GeneticVariation BEFREE Asthma susceptibility was associated with GG of the GSDMA (rs7212938) and TT of GSDMB (rs7216389). 21337730

2011

dbSNP: rs9910408
rs9910408
0.010 GeneticVariation BEFREE Asthma treatment outcome in adults is associated with rs9910408 in TBX21 gene. 24107858

2013

dbSNP: rs3204145
rs3204145
0.010 GeneticVariation BEFREE We observed a strong allelic association between BA in childhood and two of the SNP sites, T3214A (Cys1072Ser) and C3473T (Pro1158Leu); P = 0.000004 for T3214A and P = 0.0009 for C3473T. 11281413

2001

dbSNP: rs5498
rs5498
0.030 GeneticVariation BEFREE K469E showed association with asthma (P = 0.0037 with Armitage's trend test). 16625213

2006

dbSNP: rs555743307
rs555743307
0.090 GeneticVariation BEFREE I50V variants were not significantly associated with asthma. 17586032

2007

dbSNP: rs7216389
rs7216389
0.900 GeneticVariation BEFREE rs7216389 was significantly associated with the development of wheeze (hazard ratio 1.64 [1.05-2.59], P value = 0.03), asthma (hazard ratio, 1.88 [1.15-3.07], P = 0.01), and acute severe exacerbations (hazard ratio 2.66 [1.58-4.48], P value = 0.0002). 19029000

2009

dbSNP: rs200039720
rs200039720
0.010 GeneticVariation BEFREE A53T heterozygotes had a two-fold increased risk for asthma in the Copenhagen City Heart Study and Copenhagen General Population Study combined (adjusted odds ratio 2.2(1.0-4.9)). 19910179

2010

dbSNP: rs1799983
rs1799983
0.060 GeneticVariation BEFREE G894T and -786T/C polymorphisms were not associated with asthma susceptibility. 22966886

2012

dbSNP: rs2243250
rs2243250
IL4
0.060 GeneticVariation BEFREE rs2243250 and rs2227284 are significantly associated with asthma and allergic rhinitis. 23654077

2013

dbSNP: rs4795405
rs4795405
0.720 GeneticVariation BEFREE rs4795405 was strongly associated with asthma without rhinitis, a subtype of asthma for which a higher degree of airway obstruction was found. 23964555

2013

dbSNP: rs1042714
rs1042714
0.100 GeneticVariation BEFREE Gln/Glu27 polymorphism might be a contributor to asthma susceptibility for adults. 24992184

2014

dbSNP: rs11976862
rs11976862
0.010 GeneticVariation BEFREE rs11976862 homozygote mutant genotype GG was nominally associated with increased asthma risk (OR = 2.435, 95% CI: 1.221-4.854, p = 0.01148, p(corr) = 0.0127). 27133712

2016

dbSNP: rs12603332
rs12603332
0.730 GeneticVariation BEFREE rs12603332 is associated with male asthma patients specifically in urban areas of Lahore, Pakistan. 28055272

2017

dbSNP: rs721917
rs721917
0.010 GeneticVariation BEFREE Met11Thr variation strongly affected serum SP-D levels and the degree of multimerization, but was not associated with COPD and asthma in the study. 28960651

2018

dbSNP: rs1837253
rs1837253
0.840 GeneticVariation BEFREE rs1837253 is associated with asthma susceptibility and may increase the risk of asthma in Zhuang people in Guangxi. 31066119

2019

dbSNP: rs3117098
rs3117098
0.810 GeneticVariation BEFREE rs3117098 may be the risk factor for asthma in Chinese Zhuang population. 31605414

2020

dbSNP: rs6967330
rs6967330
0.060 GeneticVariation BEFREE A <i>CDHR3</i> SNP (rs6967330) with G to A base change has been linked to severe exacerbations of asthma and increased susceptibility to RV-C infections in young children. 30916989

2019

dbSNP: rs2233407
rs2233407
0.010 GeneticVariation BEFREE A -673A>T (rs2233407) was associated with asthma development in subjects with atopic asthma (odds ratio = 0.56, p = 0.004). 20674643

2010

dbSNP: rs324011
rs324011
0.040 GeneticVariation BEFREE A case-control study for association of STAT6 polymorphisms rs4559 and rs324011 with asthma risk was performed. 30511616

2018

dbSNP: rs4559
rs4559
0.010 GeneticVariation BEFREE A case-control study for association of STAT6 polymorphisms rs4559 and rs324011 with asthma risk was performed. 30511616

2018

dbSNP: rs11558538
rs11558538
0.030 GeneticVariation BEFREE A common functional single nucleotide polymorphism (SNP) within the HNMT gene (C314T) was recently related to asthma. 15693910

2005

dbSNP: rs366510
rs366510
C3
0.010 GeneticVariation BEFREE A five-SNP window between markers rs10402876 and rs366510 provided strongest evidence for linkage in the presence of linkage disequilibrium for asthma, high log[total IgE], and high log[IL-13]/[log[IFN-gamma] in terms of global P-values (P = 0.00027, 0.00013, and 0.003, respectively). 16355111

2006

dbSNP: rs2243250
rs2243250
IL4
0.060 GeneticVariation BEFREE A four-way gene-gene interaction model consisting of IL13 rs20541, IL4 rs2243250</span>, ADRB2 rs1042713, and FCER1B rs569108 was chosen as the optimal one for determining asthma susceptibility (testing balanced accuracy = 0.6089, cross-validation consistency = 10/10, P = 6.98E-05). 26613553

2016

dbSNP: rs1042713
rs1042713
0.100 GeneticVariation BEFREE A four-way gene-gene interaction model consisting of IL13 rs20541, IL4 rs2243250, ADRB2 rs1042713, and FCER1B rs569108 was chosen as the optimal one for determining asthma susceptibility (testing balanced accuracy = 0.6089, cross-validation consistency = 10/10, P = 6.98E-05). 26613553

2016

dbSNP: rs11252394
rs11252394
A 0.700 GeneticVariation GWASCAT A genome-wide association study of bronchodilator response in asthmatics. 23508266

2014