{{Rsnum
|rsid=80338894
|Chromosome=15
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FAH
|position=80158170
|Gene_s=FAH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=15
|CLNACC=RCV000020126.2
|CLNALLE=1
|CLNDBN=Tyrosinemia type I
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT:SNOMED_CT
|CLNDSDBID=NBK1515:C0268490:276700:882:124536006:410056006
|CLNHGVS=NC_000015.9:g.80450512G>T
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1515
|Disease=Tyrosinemia type I
|FwdALT=T
|FwdREF=G
|GENEINFO=FAH:2184
|GENE_ID=2184
|GENE_NAME=FAH
|REF=G
|RSPOS=80450512
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050360000000000002110100
|WGT=0
|dbSNPBuildID=131
|rsid=80338894
}}