{{Rsnum
|rsid=387906561
|Chromosome=9
|position=12694103
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=TYRP1
|Gene_s=TYRP1
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=C
|CHROM=9
|CLNACC=RCV000019163.26
|CLNALLE=1
|CLNDBN=Oculocutaneous albinism type 3
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1859932:203290:79433
|CLNHGVS=NC_000009.11:g.12694103delT
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=115501.0005
|Disease=Oculocutaneous albinism type 3
|FwdREF=T
|REF=CT
|RSPOS=12694100
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906561
|GENEINFO=TYRP1:7306
|GENE_ID=7306
|GENE_NAME=TYRP1
}}