{{Rsnum
|rsid=281865527
|Chromosome=11
|position=89191311
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=TYR
|Gene_s=TYR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=AC
|CHROM=11
|CLNACC=RCV000003969.2; RCV000085980.1
|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.88924479dupC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNSRCID=606933.0001; 606933.0027; RISN-TYR:c.929dupC
|Disease=Oculocutaneous albinism type 1A; not provided
|FwdALT=C
|REF=A
|RSPOS=88924475
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;SLO;OTHERKG;LSD
|VC=DIV
|VP=0x050360000000000002100200
|WGT=0
|dbSNPBuildID=137
|rsid=281865527
|GENEINFO=TYR:7299
|GENE_ID=7299
|GENE_NAME=TYR
}}