Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: rs17576
rs17576
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.020 GeneticVariation BEFREE Heritable polymorphisms modulate metastatic efficiency in Cancer Single nucleotide polymorphisms (SNPs) in MMP9 (rs17576) and SIPA1 (rs746429, rs931127) have been associated with nodal metastases in multiple cancers. 19906411

2010

dbSNP: rs17576
rs17576
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.020 GeneticVariation BEFREE Our data suggest that the MMP1 -1607 1G/2G, MMP2 -1306 C/T, MMP2 -1575 G/A, and MMP9 Q279R polymorphisms themselves are unlikely major risk factors among Caucasian patients with either POAG or XFG. 20808730

2010

dbSNP: rs17576
rs17576
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.020 GeneticVariation BEFREE The aim of the current case-control study was to investigate the association of four single nucleotide polymorphisms (SNPs) in MMP-9 gene: -1562 C/T, 2003 G/A (R668Q), 836 A/G (Q279R) and 1721 C/G (R574P) with BD risk in the Tunisian population. 25639450

2015

dbSNP: rs17576
rs17576
CUI: C0158266
Disease: Intervertebral Disc Degeneration
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

dbSNP: rs17576
rs17576
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.020 GeneticVariation BEFREE Our meta-analysis demonstrates that MMP-9 rs17576 G > A polymorphism might be a protective factor against the development of glaucoma in Caucasian population. 28431514

2017

dbSNP: rs17576
rs17576
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.020 GeneticVariation BEFREE In contrast, for MMP-2 15918 T>C (rs243847), MMP-2 -753 C>T (rs2285053), MMP-7 -181 A>G (rs11568818), MMP-9 -1562 C>T (rs3918242) and MMP-9 R279Q (rs17576) polymorphisms, no association was found in overall comparison, but in subgroup analyses based on source of control, stage of endometriosis, or ethnicity. 27620811

2016

dbSNP: rs17576
rs17576
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.020 GeneticVariation BEFREE The results suggest that rs17576 was not associated with glaucoma risk based on current publications. 26872021

2016

dbSNP: rs17576
rs17576
CUI: C0281899
Disease: Prolapsed lumbar disc
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

dbSNP: rs17576
rs17576
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.020 GeneticVariation BEFREE In the two-locus haplotype analyses using the four single nucleotide polymorphisms (SNPs), an increase in the distribution of the R279Q/P574R (2678G>A/4859C>G) (AC haplotype: odds ratio [OR] = 3.180, 95% confidence interval [CI] = 1.956-5.170; GG haplotype: OR = 4.374, 95% CI = 2.376-8.053) and -1562C>T/R668Q (-1562C>T/5546G>A) (CA haplotype: OR = 3.280, 95% CI = 1.406-7.653) haplotypes was significantly associated with endometriosis. 18554596

2009

dbSNP: rs17576
rs17576
CUI: C0281899
Disease: Prolapsed lumbar disc
Prolapsed lumbar disc
0.020 GeneticVariation BEFREE Further, a missense SNP in MMP9 (Q279R; rs17576) is also strongly associated with LDH in the Japanese population (p = 0.00049) and shows a combinatorial effect with THBS2 (odds ratio 3.03, 95% confidence interval 1.58-5.77). 18455130

2008

dbSNP: rs17576
rs17576
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.020 GeneticVariation BEFREE C1562T and R279Q polymorphisms are associated with the susceptibility to premature MI, but cannot predict long-term cardiac events in these patients. 28453874

2018

dbSNP: rs17576
rs17576
CUI: C0158266
Disease: Intervertebral Disc Degeneration
Intervertebral Disc Degeneration
0.020 GeneticVariation BEFREE Two alleles were significantly associated with disc degeneration: IL-6 rs1800797 and MMP-9 rs17576 and one proved to be protective: IL-6 rs1800795. 28551829

2017

dbSNP: rs17576
rs17576
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 GeneticVariation BEFREE Heritable polymorphisms modulate metastatic efficiency in Cancer Single nucleotide polymorphisms (SNPs) in MMP9 (rs17576) and SIPA1 (rs746429, rs931127) have been associated with nodal metastases in multiple cancers. 19906411

2010

dbSNP: rs17576
rs17576
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.020 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: C0022578
Disease: Keratoconus
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

dbSNP: rs17576
rs17576
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.020 GeneticVariation BEFREE our study suggests a significant association of the MMP-9 rs17576 A/G polymorphism with increased risk of BD development in Egyptian patients. 28388268

2017

dbSNP: rs17576
rs17576
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 GeneticVariation BEFREE Heritable polymorphisms modulate metastatic efficiency in Cancer Single nucleotide polymorphisms (SNPs) in MMP9 (rs17576) and SIPA1 (rs746429, rs931127) have been associated with nodal metastases in multiple cancers. 19906411

2010

dbSNP: rs17576
rs17576
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.020 GeneticVariation BEFREE The -1562C>T or R2</span>79Q polymorphism of MMP-9 gene and smoking have a synergistic effect and are significantly associated with the risk of MI in Chinese Uighur population, respectively. 21733941

2012

dbSNP: rs17576
rs17576
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.020 GeneticVariation BEFREE These findings indicate that the potentially functional polymorphisms, MMP-9 P574R and R279Q, may confer the biomarker in the occurrence and metastasis of primary lung cancer. 16061858

2005

dbSNP: rs17576
rs17576
CUI: C0022578
Disease: Keratoconus
Keratoconus
0.020 GeneticVariation BEFREE Our findings showed that the rs55703767G/T polymorphism decreased the risk of KC (OR = 0.26, 95% CI = 0.08-0.82, P = 0.022). rs17576A/G, associated with KC and the A allele, was significantly overrepresented in healthy individuals. rs6609533A/G (X-chromosome) increased the risk of KC in females (OR = 2.27, 95% CI = 1.06-4.76, P = 0.036). 28197741

2017