{{Rsnum
|rsid=4898
|Gene=TIMP1
|Chromosome=X
|position=47585586
|Orientation=plus
|GMAF=0.4504
|Gene_s=MIR4769,SYN1,TIMP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 40.0 | 26.2 | 33.8
| HCB | 33.3 | 31.1 | 35.6
| JPT | 34.1 | 25.0 | 40.9
| YRI | 36.5 | 22.2 | 41.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 33.3 | 31.1 | 35.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=23813847
|Title=The association of genetic variants of matrix metalloproteinases with abdominal aortic aneurysm: a systematic review and meta-analysis
}}

{{PMID Auto
|PMID=23841813
|Title=TIMP-1 polymorphisms in a Chinese Han population with intracerebral hemorrhage
}}

{{PMID Auto
|PMID=14988809
|Title=A dual phenotype of periventricular nodular heterotopia and frontometaphyseal dysplasia in one patient caused by a single FLNA mutation leading to two functionally different aberrant transcripts.
|OA=1
}}

{{PMID Auto
|PMID=22820628
|Title=Association of TIMP-1 +372 SNP with digital ulcer manifestation in female systemic sclerosis patients.
}}

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