rs17576, MMP9

N. diseases: 73
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.060 GeneticVariation BEFREE And some studies have reported that the G allele of rs17576 might be associated with CAD. 23819814 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.060 GeneticVariation BEFREE We explored the association of MMP2 (C-735T, rs2285053), MMP7 (A-181G, rs11568818) and MMP9 (R279Q, rs17576), (P574R, rs2250889), (R668Q, rs17577) genetic variants with LVD in coronary artery disease (CAD) patients. 22664146 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.060 GeneticVariation BEFREE This meta-analysis provided evidence that genetic polymorphism of MMP1-1607 1G/2G, MMP3-Gly45lys, MMP3-376 G/C, MMP3-1171 5A/6A, MMP9-1562 C/T and MMP9-R279Q have a small to medium effect on incidence of coronary disease. 22226810 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.060 GeneticVariation BEFREE The promoter -1562C/T and exon 6 R279Q A/G polymorphisms were determined in 1001 patients with angiographically verified stable CAD and in 204 healthy controls. 21963461 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.060 GeneticVariation BEFREE These findings suggest that MMP-9 R279Q, P574R and R668Q may have combined effect in the occurrence of CAD and -1562 CT/TT genotypes may contribute to CAD in diabetics and MI in CAD patients. 19283512 2010
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.060 GeneticVariation BEFREE The aim of this study was to analyze the occurrence of the -1612 5A/6A, -376C/G, and Glu45Lys polymorphisms of MMP3 and the -1562C/T and R279Q polymorphisms of MMP9 and their relation to the risk of coronary heart disease (CHD; stenosis >/=50% of the diameter in at least one major coronary artery) in a Chinese Han population. 19438845 2009
Angle Closure Glaucoma
CUI: C0017605
Disease: Angle Closure Glaucoma
0.050 GeneticVariation BEFREE Interestingly, distribution of rs17576 variant was statistically higher in both PACG and POAG cases than healthy controls. 31713905 2020
Primary angle-closure glaucoma
CUI: C0017606
Disease: Primary angle-closure glaucoma
0.050 GeneticVariation BEFREE Interestingly, distribution of rs17576 variant was statistically higher in both PACG and POAG cases than healthy controls. 31713905 2020
Angle Closure Glaucoma
CUI: C0017605
Disease: Angle Closure Glaucoma
0.050 GeneticVariation BEFREE Significant heterogeneity between non-Chinese and Chinese datasets precluded overall meta-analysis for rs17576 and rs3918249 (Q = 0.001 and 0.04 respectively). rs17577 was nominally associated with PACG in one Caucasian study (OR = 1.71, P = 0.02), but not in 3 Chinese studies including our study (ORs = 1.20, P = 0.07). 27272641 2016
Primary angle-closure glaucoma
CUI: C0017606
Disease: Primary angle-closure glaucoma
0.050 GeneticVariation BEFREE Significant heterogeneity between non-Chinese and Chinese datasets precluded overall meta-analysis for rs17576 and rs3918249 (Q = 0.001 and 0.04 respectively). rs17577 was nominally associated with PACG in one Caucasian study (OR = 1.71, P = 0.02), but not in 3 Chinese studies including our study (ORs = 1.20, P = 0.07). 27272641 2016
Primary angle-closure glaucoma
CUI: C0017606
Disease: Primary angle-closure glaucoma
0.050 GeneticVariation BEFREE Our data suggest that the MMP1 rs1799750 (-1607 1G/2G) and MMP9 rs17576 polymorphisms might be of value for further study as potential gender-dependent risk factors for developing POAG and PACG, respectively, in Pakistan. 23441116 2013
Angle Closure Glaucoma
CUI: C0017605
Disease: Angle Closure Glaucoma
0.050 GeneticVariation BEFREE Our data suggest that the MMP1 rs1799750 (-1607 1G/2G) and MMP9 rs17576 polymorphisms might be of value for further study as potential gender-dependent risk factors for developing POAG and PACG, respectively, in Pakistan. 23441116 2013
Primary angle-closure glaucoma
CUI: C0017606
Disease: Primary angle-closure glaucoma
0.050 GeneticVariation BEFREE This study demonstrates an association between MMP9 SNPs rs3918249 and rs17576 and PACG in the Australian population, suggesting MMP9 may be involved in the pathogenesis of this blinding disease. 21655354 2011
Angle Closure Glaucoma
CUI: C0017605
Disease: Angle Closure Glaucoma
0.050 GeneticVariation BEFREE This study demonstrates an association between MMP9 SNPs rs3918249 and rs17576 and PACG in the Australian population, suggesting MMP9 may be involved in the pathogenesis of this blinding disease. 21655354 2011
Angle Closure Glaucoma
CUI: C0017605
Disease: Angle Closure Glaucoma
0.050 GeneticVariation BEFREE In contrast, the SNP rs17576 in MMP-9 might not be related to PACG in the same population. 19633731 2009
Primary angle-closure glaucoma
CUI: C0017606
Disease: Primary angle-closure glaucoma
0.050 GeneticVariation BEFREE In contrast, the SNP rs17576 in MMP-9 might not be related to PACG in the same population. 19633731 2009
Asthma
CUI: C0004096
Disease: Asthma
0.030 GeneticVariation BEFREE Published data on the association between <i>MMP-9</i> polymorphisms (-1562 C > T, rs3918242; Gln279Arg, rs17576 Arg668Gln, rs17577) and asthma susceptibility are inconclusive. 30931075 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.030 GeneticVariation BEFREE The meta-analysis of the R279Q polymorphism, including 6 studies with 6,983 cases and 3,282 controls, showed that the R279Q polymorphism was not associated with CHD (p = 0.16). 23328249 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.030 GeneticVariation BEFREE This meta-analysis provided evidence that genetic polymorphism of MMP1-1607 1G/2G, MMP3-Gly45lys, MMP3-376 G/C, MMP3-1171 5A/6A, MMP9-1562 C/T and MMP9-R279Q have a small to medium effect on incidence of coronary disease. 22226810 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.030 GeneticVariation BEFREE The aim of this study was to analyze the occurrence of the -1612 5A/6A, -376C/G, and Glu45Lys polymorphisms of MMP3 and the -1562C/T and R279Q polymorphisms of MMP9 and their relation to the risk of coronary heart disease (CHD; stenosis >/=50% of the diameter in at least one major coronary artery) in a Chinese Han population. 19438845 2009
Asthma
CUI: C0004096
Disease: Asthma
0.030 GeneticVariation BEFREE MMP-9 -1562C>T and 836G>A (Arg279Gln) were not associated with asthma (p> or =0.15) or asthma severity (p> or =0.13), and TIMP-1 434T>C (Phe124Phe) was not associated with asthma in women (p = 0.094) or men (p = 0.207). 16061701 2005
Asthma
CUI: C0004096
Disease: Asthma
0.030 GeneticVariation BEFREE We were interested in whether the polymorphisms -T1702A, -C1562T, R279Q and +C6T within the matrix metalloproteinase 9 (MMP-9) gene were associated with asthma in a population of 231 asthmatic children.However, we found no association. 16026590 2005
Keratoconus
CUI: C0022578
Disease: Keratoconus
0.020 GeneticVariation BEFREE <b>Conclusions</b>: This study supports the hypothesis of a functional role for <i>COL4A3</i> (rs55703767, G/T), <i>MMP-9</i> (rs17576, A/G) and <i>TIMP-1</i> (rs6609533, A/G) SNPs in the pathogenesis of keratoconus. 31397194 2020
Intervertebral Disc Degeneration
CUI: C0158266
Disease: Intervertebral Disc Degeneration
0.020 GeneticVariation BEFREE Furthermore, the G allele of rs17576 was found to correlate with more severe grades of disc degeneration. 30289281 2018
Prolapsed lumbar disc
CUI: C0281899
Disease: Prolapsed lumbar disc
0.020 GeneticVariation BEFREE Our results indicated that the A allele of rs17576 reduced the risk of LDH by ∼23% on average. 30289281 2018