{{Rsnum
|rsid=61753190
|Chromosome=11
|Orientation=plus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=TYR
|position=89178239
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TYR
}}{{omim
|id=606933
|rsnum=61753190
|variant=0018
}}

{{ClinVar
|rsid=61753190
|Reversed=0
|FwdREF=CAT
|FwdALT=A
|REF=C
|ALT=CA
|RSPOS=88911406
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110200
|GENEINFO=TYR:7299
|GENE_NAME=TYR
|GENE_ID=7299
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=
NC_000011.9:g.88911407dupA
|CLNORIGIN=1
|CLNSRCID=
606933.0018
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000003991.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDBN=Oculocutaneous albinism type 1A
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1166:C0268494:203100:352731:79431:6483008
|CLNSRC=OMIM Allelic Variant
|Disease=Oculocutaneous albinism type 1A
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}