Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1042714
rs1042714
0.100 GeneticVariation BEFREE Asthmatics heterozygous for Gln/Glu27 had significantly later asthma onsets than those homozygous for Gln27. 10524541

1999

dbSNP: rs79908535
rs79908535
0.020 GeneticVariation BEFREE A novel variant of human IL-13, Gln110Arg, on chromosome 5q31, associated with asthma rather than IgE levels in case-control populations from Britain and Japan [peak odds ratio (OR) = 2.31, 95% CI 1.33-4.00]; the variant also predicted asthma and higher serum IL-13 levels in a general, Japanese paediatric population. 10699178

2000

dbSNP: rs1051931
rs1051931
0.010 GeneticVariation BEFREE The Ile198Thr and Ala379Val variants of plasmatic PAF-acetylhydrolase impair catalytical activities and are associated with atopy and asthma. 10733466

2000

dbSNP: rs1320896171
rs1320896171
0.010 GeneticVariation BEFREE The Ile198Thr and Ala379Val variants of plasmatic PAF-acetylhydrolase impair catalytical activities and are associated with atopy and asthma. 10733466

2000

dbSNP: rs1805018
rs1805018
0.010 GeneticVariation BEFREE The Ile198Thr and Ala379Val variants of plasmatic PAF-acetylhydrolase impair catalytical activities and are associated with atopy and asthma. 10733466

2000

dbSNP: rs4523
rs4523
0.030 GeneticVariation BEFREE Association studies of 33 single nucleotide polymorphisms (SNPs) in 29 candidate genes for bronchial asthma: positive association a T924C polymorphism in the thromboxane A2 receptor gene. 10830912

2000

dbSNP: rs1042713
rs1042713
0.100 GeneticVariation BEFREE Neither the Arg16Gly nor Gln27Glu polymorphisms showed evidence of linkage to qualitative measures of asthma and bronchial hyperresponsiveness (BHR) (p > 0.10) or to quantitative measures of serum IgE and airway reactivity (p > 0.10). 10934093

2000

dbSNP: rs1042714
rs1042714
0.100 GeneticVariation BEFREE Neither the Arg16Gly nor Gln27Glu polymorphisms showed evidence of linkage to qualitative measures of asthma and bronchial hyperresponsiveness (BHR) (p > 0.10) or to quantitative measures of serum IgE and airway reactivity (p > 0.10). 10934093

2000

dbSNP: rs10800812
rs10800812
T 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000

dbSNP: rs1229598
rs1229598
C 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000

dbSNP: rs17064520
rs17064520
C 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000

dbSNP: rs2153101
rs2153101
T 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000

dbSNP: rs2538026
rs2538026
T 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000

dbSNP: rs4436440
rs4436440
T 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000

dbSNP: rs4950929
rs4950929
A 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000

dbSNP: rs545854
rs545854
G 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000

dbSNP: rs946263
rs946263
A 0.700 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000

dbSNP: rs1538660
rs1538660
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: 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: rs4987053
rs4987053
0.020 GeneticVariation BEFREE In conclusion, a significant association between asthma and CCR3 T51C polymorphism localized on chromosome 3p21 was found. 11307756

2001

dbSNP: rs1042713
rs1042713
0.100 GeneticVariation BEFREE Recent studies have suggested that two polymorphisms of the beta(2)-adrenergic receptor (beta(2)AR) gene at codons 16 (arginine to glycine) and 27 (glutamine to glutamate) affect an individual's airway responsiveness, or response to acute or chronic beta(2)-agonist therapy but are not risk factors for asthma. 11371409

2001

dbSNP: rs1042714
rs1042714
0.100 GeneticVariation BEFREE Recent studies have suggested that two polymorphisms of the beta(2)-adrenergic receptor (beta(2)AR) gene at codons 16 (arginine to glycine) and 27 (glutamine to glutamate) affect an individual's airway responsiveness, or response to acute or chronic beta(2)-agonist therapy but are not risk factors for asthma. 11371409

2001

dbSNP: rs1805014
rs1805014
0.010 GeneticVariation BEFREE The central objective of this study was to elucidate the role of the Ser786Pro polymorphism in asthma and its impact on IL-4R function. 11513543

2001

dbSNP: rs76863441
rs76863441
0.020 GeneticVariation BEFREE Although lack of PAFAH activity is thought to be a risk factor for asthma, there are conflicting findings concerning association between the Val279Phe variant and asthma. 11916011

2002

dbSNP: rs4523
rs4523
0.030 GeneticVariation BEFREE The T924C polymorphism in the TBXA2R gene was recently found to be associated with asthma in Japanese adults but not in children. 12000493

2002