MMP3, matrix metallopeptidase 3, 4314

N. diseases: 473; N. variants: 24
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3025058
rs3025058
Entrez Id: 4314
Gene Symbol: MMP3
MMP3
CUI: C0027051
Disease:
Myocardial Infarction
0.020 GeneticVariation BEFREE Similar distributions of rs1799750 and rs3025058 were observed in both groups; however, the MMP9 rs3918242 T allele and the CT genotype were associated with the risk of developing MI (OR = 2.32, pC = 0.02 and OR = 2.40, pC = 0.02, respectively). 26985929 2016
dbSNP: rs3025058
rs3025058
Entrez Id: 4314
Gene Symbol: MMP3
MMP3
CUI: C0027051
Disease:
Myocardial Infarction
0.020 GeneticVariation BEFREE Genotype distributions of haplotype-tagging single nucleotide polymorphisms (rs522616, rs650108, rs569444, rs635746) and rs3025058 were not significantly different between a group with MI (n=3657) and a control group (n=1211) (p> or =0.24). 19762026 2010
dbSNP: rs569444
rs569444
Entrez Id: 4314;100288077
Gene Symbol: MMP3;WTAPP1
MMP3;WTAPP1
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE Genotype distributions of haplotype-tagging single nucleotide polymorphisms (rs522616, rs650108, rs569444, rs635746) and rs3025058 were not significantly different between a group with MI (n=3657) and a control group (n=1211) (p> or =0.24). 19762026 2010