{{Rsnum
|rsid=137854890
|Chromosome=11
|position=89178225
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TYR
|Gene_s=TYR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=11
|CLNALLE=1
|CLNDBN=Oculocutaneous albinism type 1A
|CLNDSDB=OMIM
|CLNDSDBID=203100
|CLNHGVS=NC_000011.9:g.88911393G>A
|CLNSIG=5
|Disease=Oculocutaneous albinism type 1A
|FwdALT=A
|FwdREF=G
|GENEINFO=TYR:7299
|GENE_ID=7299
|GENE_NAME=TYR
|REF=G
|RSPOS=88911393
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a01000002110100
|WGT=1
|dbSNPBuildID=133
|rsid=137854890
}}