Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113624356
rs113624356
G 0.700 CausalMutation CLINVAR

dbSNP: rs113993959
rs113993959
T 0.700 CausalMutation CLINVAR

dbSNP: rs1178187217
rs1178187217
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1294950721
rs1294950721
A 0.700 CausalMutation CLINVAR

dbSNP: rs137854539
rs137854539
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1441937959
rs1441937959
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554317002
rs1554317002
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555549674
rs1555549674
G 0.700 CausalMutation CLINVAR

dbSNP: rs201943194
rs201943194
T 0.700 CausalMutation CLINVAR

dbSNP: rs559979281
rs559979281
T 0.700 CausalMutation CLINVAR

dbSNP: rs74597325
rs74597325
T 0.700 CausalMutation CLINVAR

dbSNP: rs80359473
rs80359473
A 0.700 CausalMutation CLINVAR

dbSNP: rs863225422
rs863225422
A 0.700 GeneticVariation CLINVAR

dbSNP: rs866294686
rs866294686
T 0.700 GeneticVariation CLINVAR

dbSNP: rs869312169
rs869312169
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1042713
rs1042713
0.100 GeneticVariation BEFREE In the asthma group, one mutation (Arg16-->Gly) identified a subset of patients with a distinct clinical profile.(ABSTRACT TRUNCATED AT 250 WORDS) 8383511

1993

dbSNP: rs1042714
rs1042714
0.100 GeneticVariation BEFREE We studied beta 2-adrenoceptor genotype for the Gln/Glu 27 polymorphism and airway reactivity in 65 patients with mild to moderate asthma. 7739309

1995

dbSNP: rs1557055405
rs1557055405
A 0.700 GeneticVariation CLINVAR First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy. 9452087

1998

dbSNP: rs1300030496
rs1300030496
0.010 GeneticVariation BEFREE There was a significant difference in the frequency of I181L between white asthmatics (28%) and white control subjects (3%) (p = 0.00001), and between black control subjects (16%) and white control subjects (p = 0.002); no difference in the frequency of I181L was observed between black asthmatics (22%) and black control subjects (16%). 9817697

1998

dbSNP: rs1042713
rs1042713
0.100 GeneticVariation BEFREE We examined the beta2-adrenergic receptor (beta2AR) polymorphisms (Arg16-->Gly, Gln27-->Glu) and clinical status for 117 asthmatics. 10524541

1999

dbSNP: rs1042713
rs1042713
0.100 GeneticVariation BEFREE Polymorphisms at amino acid positions 16 (arginine to glycine) and 27 (glutamine to glutamic acid) of the beta2-adrenoreceptor (B2AR) gene are known to be functionally relevant and have been associated with more severe forms of asthma, nocturnal asthma and decreased airway responsiveness in asthmatic subjects. 10469027

1999

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: rs1042714
rs1042714
0.100 GeneticVariation BEFREE Polymorphisms at amino acid positions 16 (arginine to glycine) and 27 (glutamine to glutamic acid) of the beta2-adrenoreceptor (B2AR) gene are known to be functionally relevant and have been associated with more severe forms of asthma, nocturnal asthma and decreased airway responsiveness in asthmatic subjects. 10469027

1999

dbSNP: rs555743307
rs555743307
0.090 GeneticVariation BEFREE Our findings indicate that the Ile50Val polymorphism of IL4R does not play a substantial role in genetic predisposition for the etiology of atopy or asthma in this Japanese population. 10390422

1999

dbSNP: rs1267969615
rs1267969615
ACE
0.010 GeneticVariation BEFREE We tested a hypothesis that asthma or other atopic diseases are associated with insertion/deletion ACE, M235T angiotensinogen, and TaqI ET-1 gene polymorphisms. 10200023

1999