{{Rsnum
|rsid=104894313
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TYR
|position=89284805
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TYR
}}{{omim
|id=606933
|rsnum=104894313
|variant=0006
}}{{ClinVar
|rsid=104894313
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=89017973
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000040002110100
|GENEINFO=TYR:7299
|GENE_NAME=TYR
|GENE_ID=7299
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.89017973C>T
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=606933.0006; RISN-TYR:c.1217C>T
|CLNSIG=5
|CLNCUI=C1847024
|CLNDBN=Oculocutaneous albinism type 1B; not provided
|Disease=Oculocutaneous albinism type 1B; not provided
|CLNACC=RCV000003976.1; RCV000085913.1
|Tags=PM;S3D;SLO;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet
|CLNDSDBID=NBK1166:C1847024:606952:352731:352737:79434
}}