Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4672619
rs4672619
0.010 GeneticVariation BEFREE In conclusion, we have identified a novel SNP, rs4672619, that shows interactive effects with depression on asthma symptom severity in childhood and elderly asthmatics in opposite directions. 29973587

2018

dbSNP: rs581724
rs581724
TEK
0.010 GeneticVariation BEFREE However, SNP rs581724 was significantly associated with allergic conjunctivitis in a recessive way (p=0.007; OR=2.3 (1.3-4.4)) within the asthmatic population. 29667338

2018

dbSNP: rs591118
rs591118
0.010 GeneticVariation BEFREE This finding for rs591118 was validated successfully in both the paediatric asthma (OR 3·86, 95% CI 1·19-12·50; p=0·02) and adult COPD (2·41, 1·10-5·28; p=0·03) cohorts. 29551627

2018

dbSNP: rs60389358
rs60389358
0.010 GeneticVariation BEFREE Genetic analysis of ARG1 SNPs revealed that rs2781666 G/T genotype, T allele and C-T haplotype (rs60389358 and rs2781666) were associated with susceptibility to asthma. 30381539

2018

dbSNP: rs7044343
rs7044343
0.010 GeneticVariation BEFREE No association was found between rs7044343 variant and asthma. 28985997

2018

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: rs738409
rs738409
0.010 GeneticVariation BEFREE We describe associations that may predict ADEs, e.g., acne, high cholesterol, gout, and gallstones with rs738409 (p.I148M) in PNPLA3 and asthma with rs1990760 (p.T946A) in IFIH1. 30327483

2018

dbSNP: rs762534
rs762534
0.010 GeneticVariation BEFREE On the other hand, the minor A alleles for rs762534 and rs1800925 were not significantly associated with asthma risk. 29211635

2018

dbSNP: rs10056340
rs10056340
0.010 GeneticVariation BEFREE Inclusions of age, body mass index, and atopy in multivariate models revealed significant associations between rs10056340 (odds ratio, 2.020; 95% confidence interval, 1.283-3.180; P = .002) and all 5 17q21 SNPs and asthma in this population. 28668238

2017

dbSNP: rs1031509
rs1031509
0.010 GeneticVariation BEFREE Furthermore, having TG + GG genotypes on rs1031509 near STAT4 was associated with 5-times (95% CI, 3.03-8.55) greater odds of asthma diagnosis at the highest B[a]P range, compared to the odds at the reference range. 28807506

2017

dbSNP: rs1039559
rs1039559
0.010 GeneticVariation BEFREE For those with childhood farm exposure, carriers of the TLR6-rs1039559 T-allele (p-interaction = 0.009) and TLR6-rs5743810 C-allele (p-interaction = 0.02) were associated with lower risk of early-onset asthma. 28262750

2017

dbSNP: rs10494132
rs10494132
0.010 GeneticVariation BEFREE However, the rs10494132 polymorphism of CHIA might be a risk factor for asthma. 29233108

2017

dbSNP: rs10865710
rs10865710
0.010 GeneticVariation BEFREE Significant associations were found between rs10766197 of CYP2R1, rs7041 and rs4588 of CG, rs4646536 of CYP27B1, rs2228570, rs7975232, and rs1544410 of VDR, as well as rs1805192 and rs10865710 of PPAR and susceptibility to and prognosis of childhood bronchial asthma, providing novel targets for treating the disorder. 28590769

2017

dbSNP: rs11225138
rs11225138
0.010 GeneticVariation BEFREE The distribution of genotypes of rs11225138 and certain haplotypes of the YAP1 gene showed significant differences between different asthma severity statuses. 28293931

2017

dbSNP: rs12007907
rs12007907
0.010 GeneticVariation BEFREE In conclusion, the rs12007907 variant in IL1RAPL gene was negatively associated with asthma and IL-13 production in our study and a sex-specific association was observed in one of the validation samples. 28120837

2017

dbSNP: rs12551256
rs12551256
0.010 GeneticVariation BEFREE The G allele of IL33 SNP rs12551256 was negatively associated with asthma (OR 0.71, 95% CI: 0.53-0.94, P = 0.017). 28266165

2017

dbSNP: rs13217795
rs13217795
0.010 GeneticVariation BEFREE Herein we present the first report of the association between rs</span>13217795 and allergic rhinitis, and the first independent verification of the association between rs1321</span>7795 and asthma. 29141605

2017

dbSNP: rs1368408
rs1368408
0.010 GeneticVariation BEFREE CONCLUSIONS These results suggest that the promoter SNPs (rs6882292 and rs1368408) of SCGB3A2 gene may contribute to susceptibility to asthma in a Korean population. 28422086

2017

dbSNP: rs1384001
rs1384001
0.010 GeneticVariation BEFREE In ALSPAC, there was strong evidence for association between six SNPs and asthma: rs959974 and rs1384001 (per-allele odds ratio for both: 1.30 (95% CI: 1.15-1.47), p = 0.00001), rs7010969 (OR 1.28 (1.13-1.46), p = 0.00004), rs3735945 (OR 1.30 (1.09-1.55), p = 0.003), rs920829 (OR 1.30 (1.09-1.54), p = 0.004) and rs4738202 (OR 1.22 (1.07-1.39), p = 0.004). 27779810

2017

dbSNP: rs16969968
rs16969968
0.010 GeneticVariation BEFREE We examined the causal effect of smoking on hay fever and asthma by using the smoking-associated single nucleotide polymorphism (SNP) rs16969968/rs1051730. 28533558

2017

dbSNP: rs1883832
rs1883832
0.010 GeneticVariation BEFREE CD40 rs1883832 is associated with decreased risk of Graves' disease, especially in Asian; CD40 rs1883832 is associated with increased risk of multiple sclerosis; CD40 -1C>T (rs1883832) is not associated with the susceptibility of Hashimoto's thyroiditis, systemic sclerosis or Asthma; there is insufficient data to fully confirm the association between CD40 rs1883832 and systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), Behçet's disease (BD), myasthenia gravis (MG), Crohn's disease (CD), ulcerative colitis (UC), Sarcoidosis, Fuch uveitis syndrome (FUS), Vogt-Koyanagi-Harada syndrome (VKH), Kawasaki disease (KD), giant cell arteritis (GCA) or Immune thrombocytopenia (ITP). 29254239

2017

dbSNP: rs2070673
rs2070673
0.010 GeneticVariation BEFREE Also CYP2E1 AT + TT genotypes (rs2070673) was associated with 5-times (95% CI, 3.1-8.8) greater odds of asthma diagnosis at the highest B[a]P exposure. 28807506

2017

dbSNP: rs2227306
rs2227306
0.010 GeneticVariation BEFREE The presence of IL8-251 A/T (rs4073) and + 781C/T (rs2227306) polymorphisms was significantly associated with an increased risk of asthma (P = 0.002, P = 0.036, respectively). 28993876

2017

dbSNP: rs2381413
rs2381413
0.010 GeneticVariation BEFREE Of note, multiple SNPs in LD with rs2381413 located upstream of IL33 were significantly associated with asthma. 27177148

2017

dbSNP: rs3001978
rs3001978
0.010 GeneticVariation BEFREE In the AD patients without FLG mutations, the CC genotype of RPTN rs3001978 was associated with AD (OR 0.39, p = 0.037), early age at onset (p = 0.033), pruritus (p = 0.021), severity of AD (p = 0.045), and concomitant asthma (p = 0.041). 28219068

2017