{{Rsnum
|rsid = 28940878
|Gene = TYR
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=11
|position=89178078
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TYR
}}{{omim
|desc=ALBINISM, OCULOCUTANEOUS, TYPE IA
|id=606933
|rsnum=28940878
|variant=0019
}}
{{ neighbor
| rsid = 28940881
| distance = 124
}}
{{ neighbor
| rsid = 28940879
| distance = 39
}}

{{ClinVar
|rsid=28940878
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=88911246
|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.88911246A>G
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=606933.0019; RISN-TYR:c.125A>G
|CLNSIG=5
|CLNCUI=C0268494
|CLNDBN=Oculocutaneous albinism type 1A; not provided
|Disease=Oculocutaneous albinism type 1A; not provided
|CLNACC=RCV000003992.1; RCV000085915.1
|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}}