{{Rsnum
|rsid=281865522
|Chromosome=11
|position=89227950
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=TYR
|Gene_s=TYR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000004003.1; RCV000085905.1
|CLNALLE=1
|CLNDBN=Oculocutaneous albinism type 1A; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1166:C0268494:203100:352731:79431:6483008
|CLNHGVS=NC_000011.9:g.88961118delT
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNSRCID=606933.0029; RISN-TYR:c.1164delT
|Disease=Oculocutaneous albinism type 1A; not provided
|FwdREF=T
|REF=CT
|RSPOS=88961116
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;SLO;OTHERKG;LSD
|VC=DIV
|VP=0x050360000000000002100200
|WGT=0
|dbSNPBuildID=137
|rsid=281865522
|GENEINFO=TYR:7299
|GENE_ID=7299
|GENE_NAME=TYR
}}