{{Rsnum
|rsid=1621
|Gene=MET
|Chromosome=7
|position=116797552
|Orientation=plus
|GMAF=0.3012
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MET
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 42.5 | 49.6 | 8.0
| HCB | 77.2 | 22.1 | 0.7
| JPT | 70.8 | 26.5 | 2.7
| YRI | 25.3 | 50.7 | 24.0
| ASW | 36.8 | 43.9 | 19.3
| CHB | 77.2 | 22.1 | 0.7
| CHD | 80.7 | 16.5 | 2.8
| GIH | 61.4 | 34.7 | 4.0
| LWK | 30.3 | 45.0 | 24.8
| MEX | 50.9 | 38.6 | 10.5
| MKK | 35.9 | 52.6 | 11.5
| TSI | 43.1 | 46.1 | 10.8
| 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=19458495
|Title=Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.
|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 v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}