{{Rsnum
|rsid = 28940877
|Gene = TYR
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=11
|position=89178218
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TYR
}}{{omim
|desc=ALBINISM, OCULOCUTANEOUS, TYPE IA
|id=606933
|rsnum=28940877
|variant=0011
}}
{{ neighbor
| rsid = 28940876
| distance = 23
}}
{{ neighbor
| rsid = 1042602
| distance = 310
}}

{{ClinVar
|rsid=28940877
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=88911386
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=TYR:7299
|GENE_NAME=TYR
|GENE_ID=7299
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.88911386T>C
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=606933.0011; RISN-TYR:c.265T>C
|CLNSIG=5
|CLNCUI=C0268494
|CLNDBN=Oculocutaneous albinism type 1A; not provided
|Disease=Oculocutaneous albinism type 1A; not provided
|CLNACC=RCV000003984.1; RCV000085941.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1166:C0268494:203100:352731:79431:6483008
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}