{{Rsnum
|rsid=38857
|Gene=MET
|Chromosome=7
|position=116725359
|Orientation=plus
|GMAF=0.2332
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MET
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 48.6 | 46.8 | 4.5
| HCB | 84.4 | 15.6 | 0.0
| JPT | 72.7 | 27.3 | 0.0
| YRI | 46.1 | 46.1 | 7.8
| ASW | 47.4 | 43.9 | 8.8
| CHB | 84.4 | 15.6 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 63.3 | 33.7 | 3.1
| LWK | 53.8 | 36.8 | 9.4
| MEX | 62.5 | 32.1 | 5.4
| MKK | 54.8 | 40.0 | 5.2
| TSI | 52.0 | 40.0 | 8.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20416453
|Title=c-MET pathway involvement in chronic rhinosinusitis: a genetic association analysis
}}

{{PMID|19002214|OA=1
}} MET and autism susceptibility: family and case-control studies.

{{PMID|20011629|OA=1
}} The hepatocyte growth factor receptor (MET) gene is not associated with refractive error and ocular biometrics in a Caucasian population.

{{PMID|20080979|OA=1
}} Association of genetic variation in the MET proto-oncogene with schizophrenia and general cognitive ability.

{{PMID Auto
|PMID=24766640
|Title=Evaluation of MYOC, ACAN, HGF, and MET as Candidate Genes for High Myopia in a Han Chinese Population
}}
{{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}}