{{Rsnum
|rsid=3735520
|Gene=HGF
|Chromosome=7
|position=81771623
|Orientation=minus
|GMAF=0.4578
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=HGF
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.0 | 55.5 | 14.5
| HCB | 33.3 | 45.2 | 21.5
| JPT | 36.6 | 48.2 | 15.2
| YRI | 11.8 | 47.9 | 40.3
| ASW | 16.1 | 44.6 | 39.3
| CHB | 33.3 | 45.2 | 21.5
| CHD | 37.0 | 50.0 | 13.0
| GIH | 27.7 | 39.6 | 32.7
| LWK | 23.9 | 39.4 | 36.7
| MEX | 30.4 | 50.0 | 19.6
| MKK | 15.5 | 52.9 | 31.6
| TSI | 24.5 | 54.9 | 20.6
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19471602
|Title=Hepatocyte growth factor and myopia: Genetic association analyses in a caucasian population
|OA=1
}}

{{PMID|19060265}} High myopia is not associated with the SNPs in the TGIF, lumican, TGFB1, and HGF genes.

{{PMID|19360663|OA=1
}} Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.

{{PMID|22003120|OA=1
}} Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus.

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