{{Rsnum
|rsid=2402118
|Gene=MET
|Chromosome=7
|position=116788519
|Orientation=plus
|GMAF=0.2029
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=MET
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 13.3 | 43.4 | 43.4
| HCB | 0.0 | 15.3 | 84.7
| JPT | 0.0 | 24.8 | 75.2
| YRI | 0.0 | 2.7 | 97.3
| ASW | 3.5 | 12.3 | 84.2
| CHB | 0.0 | 15.3 | 84.7
| CHD | 0.9 | 11.0 | 88.1
| GIH | 6.9 | 35.6 | 57.4
| LWK | 0.0 | 7.3 | 92.7
| MEX | 10.3 | 37.9 | 51.7
| MKK | 3.8 | 28.8 | 67.3
| TSI | 11.8 | 48.0 | 40.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=20416453
|Title=c-MET pathway involvement in chronic rhinosinusitis: a genetic association analysis
}}

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

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

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