SNP data of: Disease - Asthma and Biological sample - CD4 T Cells

SL. No.Gene Name SNP InvolvedCommentsReference (PMID)
1STAT1rs3771300The polymorphism C39134A (rs3771300), located in a potentially cis acting regulatory element in STAT1 intron 24, was inversely related to atopy measured by skin prick test, total and specific serum IgE levels. STAT1 SNP C39134A may protect from atopic sensitization.17983380
2STAT6GT polymorphismS allele (GT13 and GT14) of the GT repeat polymorphism confers significant risks to asthma.23861779
3STAT6rs71802646Short GT repeats of rs71802646 in STAT6 contribute to higher risk for asthma.24952213
4STAT6rs324015rs324015 may have a protective effect on atopic asthma.24952213
5STAT6rs1059513rs1059513 was associated with asthma and allergic diseases.29785011
6STAT6rs3024974STAT6 C1570T polymorphism may influence lung function growth in asthmatic children.17883727
7RUNX3rs742230rs742230 was associated with asthma and allergic diseases.29785011
8GATA3rs10795656rs10795656 was associated with asthma and allergic diseases.29785011
9GATA3rs422628cg17124583 modified the association of SNP rs422628 with asthma risk at the age of 18 years. Subjects with genotype AG showed an increase in average risk ratio from 0.31 to 11.65 when methylation level increased from 0.02 to 0.12, relative to genotype AA25250096
10GATA3rs1269486The interaction between Oral Contraceptive Pill (OCP) use and SNP rs1269486 was found to be associated with the methylation level of cg17124583 in asthma.25250096
11ZBTB10rs2136016rs2136016 was associated with asthma and allergic diseases.29785011
12ZBTB10rs7009110ZBTB10 (rs7009110) was significantly associated with increased asthma with hay fever risk.24388013
13ATF3rs72756369rs72756369, associated with Diisocyanate Induced Asthma is considered most likely to function by altering gene regulatory mechanism in disease relevant cells.29969634
14ATF3rs11571537rs11571537, associated with Diisocyanate Induced Asthma is considered most likely to function by altering gene regulatory mechanism in disease relevant cells.29969634
15ATF3rs11571559rs11571559, associated with Diisocyanate Induced Asthma is considered most likely to function by altering gene regulatory mechanism in disease relevant cells.29969634
16NFKB1rs28450894The T allele of rs28450894 was significantly associated with bronchodilator drug response (BDR) in asthmatic children. The low BDR associated T allele of NFKB1 (rs28450894) is found predominantly among African populations. The low BDR associated T allele of rs28450894 is significantly associated with decreased expression of SLC39A8 in blood.29509491
17NFKB1rs4648006The T allele of rs4648006 was significantly associated with bronchodilator drug response (BDR) in asthmatic children.29509491
18IFNGrs2430561The allelic frequencies of the AA genotypes in IFNG at +874 is associated with an increased risk of asthma in the Chinese Han adult population.24995662
19IFNGCA repeat polymorphismIFNG CA repeat polymorphism confer genetic susceptibility to atopic asthma in Japanese children.11240951
20IFNGCA repeat polymorphismCA14 occurrence in the first intron of IFNG can increase the risk of asthma in the Japanese population.24995662
21IFNGrs1861494rs1861494 A/G polymorphism was associated with asthma, which may regulate the IFNgamma levels and, hence, modulate asthma pathogenesis.18385742
22TNFrs1800629The TNFα -308 (G/A) polymorphism may be associated with increased pollutant-associated effects on FEV1 intraday variability for both SO2 and NO. The A allele may increase susceptibility to the adverse effects of air pollutants.27001655
23TNFrs1800629 TNF-α - 308 G/A polymorphism was significantly correlated with the risk of asthma in West Asians.30176222
24TNFrs1799724TNF-α - 857C/T polymorphism was significantly correlated with the risk of asthma in Caucasians.30176222
25TNFrs1799964TNF-α - 1031 T/C polymorphism was significantly correlated with the risk of asthma in Caucasians and East Asians.30176222
26TNFrs361525TNF-α - 238 G/A polymorphism was significantly correlated with the risk of asthma in Caucasians.30176222
27TNFrs1800630TNF-α - 863C/A polymorphism was significantly correlated with the risk of asthma in East Asians.30176222
28TNFrs1800629TNFalpha -308 G/A polymorphism contributes to susceptibility to asthma.21082225
29TNFrs1800629Compared to the control subjects, univariate analysis showed a significant negative association of the TNFalpha -308G>A polymorphism with atopic asthma, atopic dermatitis, asthma and skin symptoms and positive SPT.27240833
30TNFrs1800629In a dominant model, TNFalpha rs1800629 SNP conferred an increased risk of Diisocyanate induced Asthma (DA).25721048
31TNFrs1800629There was a strong association between the TNFalpha gene promoter polymorphism (-308G/A) and the development to asthma in both children and adults.31161819
32TNFrs1800629TNFalpha -308A/G polymorphism is a risk factor for asthma.25668892
33TNFrs1800629TNFalpha genetic polymorphism (-308G/A) could have a role in the development of bronchial asthma among Egyptian children.30600954
34TNFrs1799724TNFalpha -857C/T polymorphism is a risk factor for asthma.25668892
35TNFrs1800629 The rs1800629 polymorphism in TNF-α was a risk factor for asthma.24936650
36TNFrs1800629Genetic variation in TNF-α-308G/A may contribute to childhood asthma and wheezing.23376082
37TNFrs1800630The TNFA-863C > A polymorphism in the promoter region of TNFA may influence TNF-alpha expression and affect TsIgE levels and susceptibility to asthma.16728705
38TNFrs1800629An association between TNF-alpha G-308A (rs1800629) and asthma was noted in the North Indian population.16393721
39TNFrs1800629The TNFalpha promoter polymorphism rs1800629 (-308G/A) might be associated with severe broncho hyperresponsiveness in Korean children with asthma.17196641
40TNFrs1800629TNF-alpha -308A allele frequency was higher in asthmatics than in controls.23527710
41TNFrs361525TNF-alpha -238A allele frequency was higher in asthmatics than in controls.23527710
42FOXP3rs56066773The mutated allele of 7340C>T was significantly associated with the simultaneous presence of autoimmunity and atopy in male children.25982578
43FOXP3rs2232367A significant increase in the frequency of the mutated allele of 1651C>T in the male control group as compared to patients with atopy and autoimmunity.25982578