{{Rsnum
|rsid=121965075
|Chromosome=15
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FAH
|position=80181048
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FAH
}}{{omim
|id=276700
|rsnum=121965075
|variant=0004
}}{{ClinVar
|rsid=121965075
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=80473390
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FAH:2184
|GENE_NAME=FAH
|GENE_ID=2184
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.80473390G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=613871.0004
|CLNSIG=5
|CLNCUI=C0268490
|CLNDBN=Tyrosinemia type I
|Disease=Tyrosinemia type I
|CLNACC=RCV000012646.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT:SNOMED_CT
|CLNDSDBID=NBK1515:C0268490:276700:882:124536006:410056006
}}