Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17576
rs17576
CUI: C1956346
Disease: Coronary Artery 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

dbSNP: rs17576
rs17576
CUI: C1956346
Disease: Coronary Artery 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

dbSNP: rs17576
rs17576
CUI: C0017606
Disease: Primary angle-closure glaucoma
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

dbSNP: rs17576
rs17576
CUI: C0017605
Disease: Angle Closure Glaucoma
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

dbSNP: rs17576
rs17576
CUI: C0017606
Disease: Primary angle-closure glaucoma
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

dbSNP: rs17576
rs17576
CUI: C0017605
Disease: Angle Closure Glaucoma
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

dbSNP: rs17576
rs17576
CUI: C0017606
Disease: Primary angle-closure glaucoma
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

dbSNP: rs17576
rs17576
CUI: C0017605
Disease: Angle Closure Glaucoma
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

dbSNP: rs17576
rs17576
CUI: C0017605
Disease: Angle Closure Glaucoma
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

dbSNP: rs17576
rs17576
CUI: C0017605
Disease: Angle Closure Glaucoma
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

dbSNP: rs17576
rs17576
CUI: C0017606
Disease: Primary angle-closure glaucoma
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

dbSNP: rs17576
rs17576
CUI: C0017606
Disease: Primary angle-closure glaucoma
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

dbSNP: rs17577
rs17577
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.030 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

dbSNP: rs17577
rs17577
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.030 GeneticVariation BEFREE AT1 A1166C independently and in combination with MMP9 R668Q and NFKB1-94 ATTG ins/del polymorphisms plays important role in conferring genetic susceptibility to LVD in CAD patients. 24875414

2014

dbSNP: rs17577
rs17577
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.030 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

dbSNP: rs17576
rs17576
CUI: C0010068
Disease: Coronary heart 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

dbSNP: rs17576
rs17576
CUI: C0004096
Disease: Asthma
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

dbSNP: rs17576
rs17576
CUI: C0004096
Disease: Asthma
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

dbSNP: rs17576
rs17576
CUI: C0004096
Disease: Asthma
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

dbSNP: rs17576
rs17576
CUI: C0010068
Disease: Coronary heart 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

dbSNP: rs17576
rs17576
CUI: C0010068
Disease: Coronary heart 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

dbSNP: rs3918249
rs3918249
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.020 GeneticVariation BEFREE Significant associations were only found between MMP-9 rs17576 G > A polymorphism (GA vs. GG: OR = 0.80, 95%CI = 0.67-0.97, P = 0.02, I<sup>2</sup> = 0%), MMP-9 rs3918249 C > T polymorphism (TT vs. CC + CT: OR = 0.71, 95%CI = 0.51-0.98, P = 0.04, I<sup>2</sup> = 0%) and glaucoma risk in the general population. 28431514

2017

dbSNP: rs3918249
rs3918249
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma
0.020 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

dbSNP: rs3918249
rs3918249
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma
0.020 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

dbSNP: rs3918249
rs3918249
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma
0.020 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