{{Rsnum
|rsid=61754393
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TYR
|position=89284853
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TYR
}}{{omim
|id=606933
|rsnum=61754393
|variant=0012
}}{{ClinVar
|rsid=61754393
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=89018021
|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.89018021G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000003985.1; RCV000085916.1
|CLNDBN=Oca1-ts; not provided
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNSRCID=606933.0012; RISN-TYR:c.1265G>A
|Disease=Oca1-ts; not provided
}}