{{Rsnum
|rsid=104894318
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TYR
|position=89284930
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TYR
}}{{omim
|id=606933
|rsnum=104894318
|variant=0032
}}{{ClinVar
|rsid=104894318
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=89018098
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=TYR:7299
|GENE_NAME=TYR
|GENE_ID=7299
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.89018098G>A
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=606933.0032; RISN-TYR:c.1342G>A
|CLNSIG=5
|CLNCUI=C0268494
|CLNDBN=Oculocutaneous albinism type 1A; not provided
|Disease=Oculocutaneous albinism type 1A; not provided
|CLNACC=RCV000004006.1; RCV000085921.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1166:C0268494:203100:352731:79431:6483008
}}