{{Rsnum
|rsid=38845
|Gene=MET
|Chromosome=7
|position=116681748
|Orientation=plus
|GMAF=0.3944
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|effect1=
|effect2=
|effect3=
|Gene_s=MET
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 16.1 | 44.6 | 39.3
| HCB | 11.9 | 56.7 | 31.3
| JPT | 17.9 | 51.8 | 30.4
| YRI | 7.0 | 43.0 | 50.0
| ASW | 10.9 | 38.2 | 50.9
| CHB | 11.9 | 56.7 | 31.3
| CHD | 22.0 | 56.9 | 21.1
| GIH | 15.8 | 40.6 | 43.6
| LWK | 0.9 | 33.9 | 65.1
| MEX | 27.3 | 52.7 | 20.0
| MKK | 3.3 | 32.7 | 64.1
| TSI | 31.4 | 40.2 | 28.4
| HapMapRevision=28
}}

[[rs38845]] is a SNP in the first intron of the transmembrane receptor tyrosine kinase of the hepatocyte growth factor/scatter factor [[MET]] gene.

{{PMID|19002214|OA=1
}} [[rs38845]] is associated with [[autism]] (p < 0.004) in a study of 325 multiplex International Molecular Genetic Study of Autism Consortium (IMGSAC) families and 10 trios

{{PMID Auto
|PMID=22110649
|Title=Replication of the Association of a MET Variant with Autism in a Chinese Han Population
|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
}}

{{PMID Auto
|PMID=20615438
|Title=Further evidence for the role of MET in autism susceptibility.
}}

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