{{Rsnum
|rsid=2889529
|Gene=TIMP2
|Chromosome=17
|position=78901393
|Orientation=minus
|GMAF=0.4573
|Gene_s=LOC100653515,TIMP2
|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 | 17.7 | 50.4 | 31.9
| HCB | 7.4 | 44.1 | 48.5
| JPT | 4.4 | 39.8 | 55.8
| YRI | 51.7 | 40.6 | 7.7
| ASW | 32.1 | 48.2 | 19.6
| CHB | 7.4 | 44.1 | 48.5
| CHD | 6.5 | 34.6 | 58.9
| GIH | 16.0 | 45.0 | 39.0
| LWK | 53.6 | 41.8 | 4.5
| MEX | 15.8 | 49.1 | 35.1
| MKK | 51.0 | 41.8 | 7.2
| TSI | 17.0 | 57.0 | 26.0
| HapMapRevision=28
}}{{omim
|desc=PONTOCEREBELLAR HYPOPLASIA TYPE 2A; PCH2A
|id=277470
|rsnum=2889529
}}

{{PMID Auto
|PMID=17903307
|Title=Framingham Heart Study genome-wide association: results for pulmonary function measures.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}