{{Rsnum
|rsid = 28940881
|Gene = TYR
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=11
|position=89177954
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TYR
}}{{omim
|desc=ALBINISM, OCULAR, AUTOSOMAL RECESSIVE
|id=606933
|rsnum=28940881
|variant=0037
}}
{{ neighbor
| rsid = 28940878
| distance = 124
}}

{{ClinVar
|rsid=28940881
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=88911122
|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.88911122A>G
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=606933.0037; RISN-TYR:c.1A>G
|CLNSIG=5
|CLNCUI=C1847024
|CLNDBN=Oculocutaneous albinism type 1B; not provided
|Disease=Oculocutaneous albinism type 1B; not provided
|CLNACC=RCV000004011.1; RCV000085931.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet
|CLNDSDBID=NBK1166:C1847024:606952:352731:352737:79434
}}

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