rs1030868
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1030868(C;C) |
| Make rs1030868(C;T) |
| Make rs1030868(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 55482855 |
| Gene | MMP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1030868 |
| dbSNP (classic) | rs1030868 |
| ClinGen | rs1030868 |
| ebi | rs1030868 |
| HLI | rs1030868 |
| Exac | rs1030868 |
| Gnomad | rs1030868 |
| Varsome | rs1030868 |
| LitVar | rs1030868 |
| Map | rs1030868 |
| PheGenI | rs1030868 |
| Biobank | rs1030868 |
| 1000 genomes | rs1030868 |
| hgdp | rs1030868 |
| ensembl | rs1030868 |
| geneview | rs1030868 |
| scholar | rs1030868 |
| rs1030868 | |
| pharmgkb | rs1030868 |
| gwascentral | rs1030868 |
| openSNP | rs1030868 |
| 23andMe | rs1030868 |
| SNPshot | rs1030868 |
| SNPdbe | rs1030868 |
| MSV3d | rs1030868 |
| GWAS Ctlg | rs1030868 |
| GMAF | 0.3655 |
| Max Magnitude | 0 |
[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
