{{Rsnum
|rsid=61753185
|Gene=TYR
|Chromosome=11
|position=89178183
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TYR
}}{{omim
|id=606933
|rsnum=61753185
|variant=0005
}}
{{omim
|id=606933
|rsnum=61753185
|variant=0010
}}

{{ClinVar
|rsid=61753185
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=88911351
|CHROM=11
|GMAF=0.0005
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000016110100
|GENEINFO=TYR:7299
|GENE_NAME=TYR
|GENE_ID=7299
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.88911351G>A
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=606933.0005; 606933.0010; RISN-TYR:c.230G>A
|CLNSIG=5
|CLNCUI=C0268494
|CLNDBN=Oculocutaneous albinism type 1A; not provided
|Disease=Oculocutaneous albinism type 1A; not provided
|CLNACC=RCV000003975.1; RCV000085934.1
|Tags=PM;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1166:C0268494:203100:352731:79431:6483008
|COMMON=0
}}

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