{{Rsnum
|rsid=2287076
|Gene=MMP2
|Chromosome=16
|position=55498546
|Orientation=plus
|GMAF=0.3444
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MMP2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 23.2 | 46.4 | 30.4
| HCB | 7.3 | 44.5 | 48.2
| JPT | 14.2 | 43.4 | 42.5
| YRI | 2.0 | 32.0 | 66.0
| ASW | 5.3 | 33.3 | 61.4
| CHB | 7.3 | 44.5 | 48.2
| CHD | 10.1 | 36.7 | 53.2
| GIH | 19.8 | 50.5 | 29.7
| LWK | 1.8 | 13.6 | 84.5
| MEX | 17.9 | 55.4 | 26.8
| MKK | 1.3 | 17.9 | 80.8
| TSI | 22.8 | 47.5 | 29.7
| HapMapRevision=28
}}

{{PMID|18560213}} association of the MMP-2 gene with the development of lacunar stroke. [[rs1030868]], [[rs2241145]], [[rs2287074]], [[rs2287076]], [[rs7201]] showed a significant association with small vessel infarcts (p < 0.05) and rs7201:g.C was identified as an independent risk factor by multivariable logistic regression analysis

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}