Record no | GENE NAME | SNP ID | CHANGES | ANCESTRAL ALLELES | FUNCTIONAL CONSEQUENCES | DISEASE | POPULATION | Pubmed ID | Comments |
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1 | MX1 | rs469390 | A/G | G | Missense Variant | Viral Respiratory Illness, Asthma | European or American European | 26399222 | rs469390, which encodes a missense mutation (G/A; Val379Ile) in exon 15 of the MX1 protein, was significantly associated with viral asthma burden in RhinoGen study and asthma exacerbations in COPSAC (Copenhagen Prospective Study on Asthma in Childhood) study. The allele (G) associated with increased viral asthma burden in the RhinoGen children, was associated with fewer asthma exacerbations in COPSAC children. |
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2 | MX1 | rs2070229 | C/T | T | Synonymous Variant | Viral Respiratory Illness, Asthma | European or American European | 26399222 | rs2070229 was significantly associated with viral asthma burden and weeks infected in RhinoGen study, with Rhinoviral wheezing in COAST (Childhood Origins of Asthma) study and with asthma exacerbations in COPSAC (Copenhagen Prospective Study on Asthma in Childhood) study. |
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3 | MX1 | rs467593 | A/G | G | Intron Variant | Viral Respiratory Illness, Asthma | European or American European | 26399222 | rs467593 was in linkage disequilibrium with rs2070229 and shows the same opposite pattern of association in RhinoGen study as compared to COPSAC (Copenhagen Prospective Study on Asthma in Childhood) study and COAST (Childhood Origins of Asthma) study. |
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4 | MRPP3 | rs12436663 | A/G | G | Intron Variant | Asthma | - | 26031901 | rs12436663 in MRPP3 was associated with worsening response to zileuton in asthmatics. Homozygous rs12436663 carriers showed a significant reduction in mean ΔFEV1 following zileuton treatment. |
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5 | miR-196a2 | rs11614913 | C/T | C | Non Coding Transcript Variant | Asthma | Korean population | 28527151 | The CT/CC genotype of miR-196a2 rs11614913 was associated with eosinophilic asthma and a higher sputum eosinophil count compared with the TT genotype. |
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6 | miR-146a | rs2910164 | C/G | G | Non Coding Transcript Variant | Asthma | Korean population | 28527151 | The CG/GG genotype of miR-146a rs2910164 was associated with higher bronchial hyperresponsiveness to methacholine compared with the CC genotype in asthmatic patients. |
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7 | miR-499 | rs3746444 | C/T | T | Non Coding Transcript Variant | Asthma | Korean population | 28527151 | The AG/GG genotype of miR-499 rs3746444 was associated with higher predicted values of forced expiratory volume in 1 s (%FEV1) compared with the AA genotype in asthmatic patients. |
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8 | miR499 | rs3746444 | G/A | A | Non Coding Transcript Variant | Bronchial Asthma | Egyptian children and adolescents | 28886711 | miR499 rs3746444 (A > G) polymorphism was associated with asthma susceptibility and bronchodilator response in Egyptian children and adolescents. The G variant was associated with high risk of developing asthma under all genetic association models. |
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9 | MMP9 | rs20544 | C/T | C | 3 Prime UTR Variant | Childhood Asthma | Slovenian population | 29600353 | There exists an association of MMP9 genotype rs20544 TT with better asthma control and indirectly better response to treatment. |
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10 | MMP9 | rs13925 | A/G | G | Synonymous Variant | Childhood Asthma | Slovenian population | 29600353 | There exists an association of MMP9 genotypes rs13925 AA and AG with better asthma control and indirectly better response to treatment. |
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11 | MUC22 | rs2523924 | A/G | A | Intron Variant | Childhood Asthma | Chinese population | 28262390 | Compared with the controls, patients were found to have significantly lower frequencies of genotype AA of rs2523924. |
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12 | MMP12 | rs2276109 | A/G (REV) | A | 2KB Upstream Variant | Bronchial Asthma | Bulgarian population | 29390099 | The variant G allele of the MMP12 -82 A>G promoter polymorphism (rs2276109) might be considered protective for development of Bronchial Asthma in ethnic Bulgarian adults residing in central Bulgaria. |
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13 | MAP4K4 | rs12468899 | A/G/T | G | Intron Variant | Asthma | European Ancestry | 27130862 | rs12468899 in 2q11-q12 loci was associated with time to asthma onse (TAO) at suggestive significance levels. |
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14 | MED24 | rs2302777 | A/G | G | Synonymous Variant | Asthma | Slovenian population | 27163155 | rs2302777 was highly associated with asthma. |
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15 | MMP2 | rs9302671 | G/T | G | Intron Variant | Asthma | European population | 27334786 | rs9302671 SNP in the MMP2 gene was associated with asthma. |
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16 | MMP2 | rs17301608 | A/C/G/T | C | Intron Variant | Asthma | European population | 27334786 | rs17301608 SNP in the MMP2 gene was associated with asthma. |
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17 | MMP9 | rs17577 | A/C/G | G | Missense Variant | Asthma | - | 30931075 | MMP-9 Arg668Gln, rs17577 polymorphism may be the risk factor for asthma susceptibility. |
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18 | MMP9 | rs17576 | A/G | A | Missense Variant | Asthma | - | 30931075 | For the Gln279Arg, rs17576 polymorphism, there seems to be a significant association with asthma susceptibility in the allelic genetic model. |
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19 | MYH15 | rs9288876 | A/T | A | Intron Variant | Asthma | Chinese Han population | 30906771 | MYH15 polymorphism of rs9288876 altered transcriptional regulation of MYH15 and may be functional variant conferring susceptibility to asthma. |
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20 | MYH15 | rs7635009 | A/G | A | Intron Variant | Asthma | Chinese Han population | 30906771 | MYH15 polymorphism of rs7635009 altered transcriptional regulation of MYH15 and may be functional variant conferring susceptibility to asthma. |
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21 | MYH15 | rs1454197 | G/T | G | Intron Variant | Asthma | Chinese Han population | 30906771 | MYH15 polymorphism of rs1454197 altered transcriptional regulation of MYH15 and may be functional variant conferring susceptibility to asthma. |
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22 | miR-196a2 | rs11614913 | C/T | C | Non Coding Transcript Variant | Asthma | Egyptian population | 27487239 | microRNA-196a2 rs11614913 polymorphism might be associated with asthma severity. |
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23 | miR-152 | rs1707 | C/T | - | - | Asthma | Chinese Han population | 27383317 | Pre-miR-152 rs1707 may contribute to the risk of asthma in a Chinese Han population. |
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24 | miR-133a1 | rs8089787 | C/T | T | 2KB Upstream Variant | Asthma | Chinese Han population | 27383317 | The CT and CT+TT genotypes in the miR-133a1 rs8089787 were significantly associated with a decreased risk for asthma in sample of the Chinese Han population, compared with CC genotype. |
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25 | miR-133a1 | rs9948906 | A/C/T | T | 2KB Upstream Variant | Asthma | Chinese Han population | 27383317 | The CT and CT+TT genotypes in the miR-133a1 rs9948906 were associated with a decreased risk of asthma. |
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26 | MAML3 | rs345983 | C/T | T | 3 Prime UTR Variant | Asthma | Dutch population | 27709636 | Minor allele of rs345983 was associated with less severe BHR and higher lung tissue gene expression. MAML3 was associated with BHR severity in adult asthma. |
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27 | miR-149 | rs2292832 | A/C/T | C | Non Coding Transcript Variant | Allergic Rhinitis with Comorbid Asthma (In Children) | Chinese population | 28181414 | miR-149 rs2292832 variant is not only strongly associated with Allergic Rhinitis and Allergic Rhinitis with Asthma, but it may lead to an increase in the susceptibility to allergies following the stimulation with an allergen, through the changes in miR-149 expression. |
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28 | MRPL44 | rs76568361 | G/T | T | - | Asthma and Allergy Traits | Saguenay Lac Saint Jean Population | 30206357 | rs76568361 was found to be associated with eosinophil percentage. |
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29 | MIF | rs755622 | C/G (REV) | G | 2KB Upstream Variant | Childhood Asthma | Egyptian population | 27833444 | MIF-173G/C (rs755622) polymorphism confers an increased risk of susceptibility to the development of childhood asthma in Egyptian population. |
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30 | mEPHX1 | - | - | - | - | Childhood Bronchial Asthma | Pre Carpathian population | 28713081 | Patients with uncontrolled asthma have genotypes CC and GG much more often. Children with asthma often have high enzymatic activity of a gene mEPHX1 (polymorphic variants of AG and AA-TT-TT). A "slow" functional state of gene mEPHX1 corresponding to homozygotes and heterozygotes for the mutant alleles: СС-АА and ТС-АА is also a frequent phenomenon. |
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31 | MMP9 | rs17576 | A/G | A | Missense Variant | Childhood Asthma | - | 27395373 | A direct correlation between MMP9 (Q279R) SNP (rs17576) and MMP9 enzyme activity was found in EBC of asthmatic children. |
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32 | MMP9 | rs17577 | A/C/G | G | Missense Variant | Childhood Asthma | - | 27395373 | A direct correlation between MMP9 (R668Q) SNP (rs17577) and MMP9 enzyme activity was found in EBC of asthmatic children. |
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33 | MICA | rs2596560 | A/G (REV) | A | 2KB Upstream Variant | Asthma | Dutch population | 27439200 | The risk allele C of rs2596560 on chromosome 6 near MICA, associated with a higher risk of atopy within asthmatics. |
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34 | MIR205HG, MIR205, LAMB3, CAMK1G | rs10746419 | C/G/T | T | - | Childhood Asthma | Puerto Rican population, Mexican population, African American population | 29509491 | The T allele of rs10746419 was significantly associated with bronchodilator drug response (BDR) in asthmatic children. |
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35 | MN1, PITPNB | rs60163793 | A/C/G | C | - | Childhood Asthma | Puerto Rican population, Mexican population, African American population | 29509491 | The G allele of rs60163793 was significantly associated with bronchodilator drug response (BDR) in asthmatic children. |
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36 | MED24 | rs7502514 | A/G | G | Intron Variant | Asthma | - | 27554816 | rs7502514 is an eQTL for MED24 gene which is significantly associated with asthma risk. |
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37 | MED12L | rs10513393 | A/G | G | Intron Variant | Asthma | - | 27554816 | rs10513393 is an eQTL for P2RY14 gene which is significantly associated with asthma risk. |
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38 | MICB | rs9268764 | C/T | T | - | Asthma | - | 27554816 | rs9268764 is an eQTL for MICB gene which is significantly associated with asthma risk. |
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39 | miR-146a | rs2910164 | C/G | G | Non Coding Transcript Variant | Bronchial hyperresponsiveness (BHR) in patients with basic pulmonary disease (such as Asthma, Emphysema and Bronchitis) | Chinese population | 27431205 | The miR-146a rs2910164 polymorphism CC genotype was identified to be significantly associated with an increased risk of Bronchial hyperresponsiveness (BHR) in response to intubation in patients exhibiting basic pulmonary disease (such as asthma, emphysema and bronchitis) when compared with the GG or GC genotype. |
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40 | MYLK | rs936170 | A/C/G | C | Intron Variant | Asthma | Korean population | 19277499 | MYLK Polymorphism (+89872C > G) was associated with blood eosinophil level among asthmatic patients in korean population. |
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41 | MYLK | 92263T >C | T/C | | - | Asthma | Korean population | 19277499 | MYLK Polymorphism (+92263T >C) was associated with blood eosinophil level among asthmatic patients in korean population. |
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42 | MYLK | rs9840993 | A/G | G | Missense Variant | Asthma | - | 25271083 | MYLK variant rs9840993 regulates asthmatic inflammation via alterations in mRNA secondary structure. |
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43 | MMP2 | rs243865 | C/T | C | 2KB Upstream Variant | Asthma | North Indian population | 24843799 | The MMP-2 -1306C/T promoter (rs243865) polymorphism confers significant protection from asthma in the studied North Indian population. |
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44 | MMP8 | rs17099451 | A/C/T | C | 2KB Upstream Variant | Bronchial Asthma | Japanese population | 24498518 | rs17099451 in MMP8 was associated with Bronchial Asthma in a Japanese Population. |
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45 | MS4A2 | rs1441586 | C/T | C | Intron Variant | Asthma | Chinese Han population | 24838642 | The MS4A2 C-109T T/T genotype was associated with asthma in the Chinese Han children. |
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