{{Rsnum
|rsid=137853235
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HGF
|position=81752250
|Gene_s=HGF
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=142409
|variant=0001
|rsnum=137853235
}}{{ClinVar
|rsid=137853235
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=81381566
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HGF:3082
|GENE_NAME=HGF
|GENE_ID=3082
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.81381566C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=142409.0001
|CLNSIG=5
|CLNCUI=C1842342
|CLNDBN=Deafness, autosomal recessive 39
|Disease=Deafness
|CLNACC=RCV000016089.21
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1842342:608265:90636
}}