Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799750
rs1799750
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 GeneticVariation BEFREE This examination, as the first study of its own kind in Iranian Turks, reported association between MMP-1 (rs1799750) -1607 2G/2G and MMP-3 (rs3025058) -1612 6A/6A genotypes and CAD risk in patients older than 50 years. 31356534

2019

dbSNP: rs1799750
rs1799750
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.020 GeneticVariation BEFREE <b>Conclusion.</b> We systematically investigated the association between MMP-1-1607 (rs1799750) 1G/2G polymorphism and OA susceptibility; however, the results show no correlation. 30886066

2019

dbSNP: rs1799750
rs1799750
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 GeneticVariation BEFREE Association of MMP-1 (rs1799750)-1607 2G/2G and MMP-3 (rs3025058)-1612 6A/6A Genotypes With Coronary Artery Disease Risk Among Iranian Turks. 31356534

2019

dbSNP: rs1799750
rs1799750
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.020 GeneticVariation BEFREE In conclusion, this case-control study confirms that <i>MMP-1</i> gene rs1799750 polymorphism increases the risk of knee OA in Chinese Han population. 30177524

2018

dbSNP: rs1799750
rs1799750
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
0.020 GeneticVariation BEFREE The association between MMP-1 gene rs1799750 polymorphism and knee osteoarthritis risk. 30177524

2018

dbSNP: rs1799750
rs1799750
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle
0.020 GeneticVariation BEFREE Subgroup analyses showed that the rs1799750 was significantly associated with primary angle closure glaucoma under homozygote (OR = 2.23, 95% CI 1.03-4.83, p = 0.043) and allelic (OR = 1.61, 95% CI 1.07-2.42, P = 0.021) models, while it was significantly associated with primary open angle glaucoma (OR = 1.64, 95% CI 1.05-2.56, p = 0.030) and exfoliation glaucoma (OR = 1.42, 95% CI 1.02-1.97, p = 0.036) under recessive models. 27428613

2017

dbSNP: rs1799750
rs1799750
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 GeneticVariation BEFREE Thus, MMP-1 rs1799750 may be involved in the development of coexisting T2DM and CHD in the Han Chinese population. 27323171

2016

dbSNP: rs1799750
rs1799750
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.020 GeneticVariation BEFREE The majority of the research described in the present mini-review proves that the genetic polymorphism in the MMP1 (rs1799750) is the most widely studied, and suggests that the rare genotype, 2G2G, of that gene might show increased susceptibility for bladder cancer, especially among smokers. 24635493

2014

dbSNP: rs1799750
rs1799750
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 GeneticVariation BEFREE Significantly more C-2G (rs498186-rs1799750) haplotypes (p=0.001 after Bonferroni corrections) were found in CAD subjects. 25372932

2014

dbSNP: rs1799750
rs1799750
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.020 GeneticVariation BEFREE The majority of the research described in the present mini-review proves that the genetic polymorphism in the MMP1 (rs1799750) is the most widely studied, and suggests that the rare genotype, 2G2G, of that gene might show increased susceptibility for bladder cancer, especially among smokers. 24635493

2014

dbSNP: rs1799750
rs1799750
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
0.020 GeneticVariation BEFREE The present study shows that MMP1 -1607 1G/2G (rs1799750) polymorphism might be a risk factor for knee osteoarthritis susceptibility in the Greek population. 24838892

2014

dbSNP: rs1799750
rs1799750
Malignant neoplasm of urinary bladder
0.020 GeneticVariation BEFREE The majority of the research described in the present mini-review proves that the genetic polymorphism in the MMP1 (rs1799750) is the most widely studied, and suggests that the rare genotype, 2G2G, of that gene might show increased susceptibility for bladder cancer, especially among smokers. 24635493

2014

dbSNP: rs1799750
rs1799750
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: rs1799750
rs1799750
Malignant neoplasm of urinary bladder
0.020 GeneticVariation BEFREE To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 (rs1799750), MMP2 (rs243865), MMP9 (rs3918242), MMP12 (rs2276109) and tissue inhibitors of MMPs (TIMPs) TIMP1 (rs2070584) and TIMP3 (rs9619311) genes that may be involved in susceptibility to bladder cancer (BC). 23819551

2013

dbSNP: rs1799750
rs1799750
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.020 GeneticVariation BEFREE To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 (rs1799750), MMP2 (rs243865), MMP9 (rs3918242), MMP12 (rs2276109) and tissue inhibitors of MMPs (TIMPs) TIMP1 (rs2070584) and TIMP3 (rs9619311) genes that may be involved in susceptibility to bladder cancer (BC). 23819551

2013

dbSNP: rs1799750
rs1799750
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.020 GeneticVariation BEFREE To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 (rs1799750), MMP2 (rs243865), MMP9 (rs3918242), MMP12 (rs2276109) and tissue inhibitors of MMPs (TIMPs) TIMP1 (rs2070584) and TIMP3 (rs9619311) genes that may be involved in susceptibility to bladder cancer (BC). 23819551

2013

dbSNP: rs1799750
rs1799750
CUI: C0263912
Disease: Rotator cuff syndrome
Rotator cuff syndrome
0.010 GeneticVariation BEFREE In conclusion, a significant correlation was identified between the MMP-1 rs1799750 polymorphism</span> and RCT. 31652448

2019

dbSNP: rs1799750
rs1799750
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE Association of MMP-1 (rs1799750)-1607 2G/2G and MMP-3 (rs3025058)-1612 6A/6A Genotypes With Coronary Artery Disease Risk Among Iranian Turks. 31356534

2019

dbSNP: rs1799750
rs1799750
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 GeneticVariation BEFREE Meta-analysis showed no associations between MMP1 rs1799750, MMP2 rs243865, or MMP7 rs11568818 and prostate cancer risk overall. 30464622

2018

dbSNP: rs1799750
rs1799750
Exudative age-related macular degeneration
0.010 GeneticVariation BEFREE MMP1 rs1799750 1G/2G genotype was found to play a significant role in the development of eAMD at the age of less than 65 years. 29947568

2018

dbSNP: rs1799750
rs1799750
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 GeneticVariation BEFREE Meta-analysis showed no associations between MMP1 rs1799750, MMP2 rs243865, or MMP7 rs11568818 and prostate cancer risk overall. 30464622

2018

dbSNP: rs1799750
rs1799750
CUI: C0035439
Disease: Rheumatic Heart Disease
Rheumatic Heart Disease
0.010 GeneticVariation BEFREE Our results suggest that rs1799750 in MMP1 might be a risk factor for RHD in a Han population in Southern China, and individuals carrying the 2G/2G genotype are likely more susceptible to RHD. 29458338

2018

dbSNP: rs1799750
rs1799750
CUI: C0206368
Disease: Exfoliation Syndrome
Exfoliation Syndrome
0.010 GeneticVariation BEFREE Subgroup analyses showed that the rs1799750 was significantly associated with primary angle closure glaucoma under homozygote (OR = 2.23, 95% CI 1.03-4.83, p = 0.043) and allelic (OR = 1.61, 95% CI 1.07-2.42, P = 0.021) models, while it was significantly associated with primary open angle glaucoma (OR = 1.64, 95% CI 1.05-2.56, p = 0.030) and exfoliation glaucoma (OR = 1.42, 95% CI 1.02-1.97, p = 0.036) under recessive models. 27428613

2017

dbSNP: rs1799750
rs1799750
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.010 GeneticVariation BEFREE The aim of this study was to examine the association between MMP1-1607dupG (rs1799750) and MMP3-1171dupA (rs3025058) gene polymorphisms and acute coronary syndromes (ACS) in the form of unstable angina. 29044936

2017

dbSNP: rs1799750
rs1799750
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.010 GeneticVariation BEFREE Subjects with MMP-1 rs1799750 polymorphism had an decreased N</span>PC risk (OR = 0.79; 95%CI, 0.69-0.91; P = 0.0007; I2 = 70%). 29096757

2017