{{Rsnum
|rsid=2286194
|Gene=HGF
|Chromosome=7
|position=81726133
|Orientation=plus
|GMAF=0.1979
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=HGF
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 2.7 | 26.5 | 70.8
| HCB | 5.1 | 28.5 | 66.4
| JPT | 1.8 | 34.5 | 63.7
| YRI | 2.0 | 32.0 | 66.0
| ASW | 3.5 | 29.8 | 66.7
| CHB | 5.1 | 28.5 | 66.4
| CHD | 1.9 | 35.2 | 63.0
| GIH | 3.0 | 35.6 | 61.4
| LWK | 5.5 | 41.8 | 52.7
| MEX | 6.9 | 37.9 | 55.2
| MKK | 12.8 | 44.2 | 42.9
| TSI | 2.0 | 40.6 | 57.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=19471602
|Title=Hepatocyte growth factor and myopia: Genetic association analyses in a caucasian population
|OA=1
}}

{{PMID|19576567|OA=1
}} Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}