{{Rsnum
|rsid=121912778
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TYRP1
|position=12704564
|Gene_s=TYRP1
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
}}{{omim
|id=115501
|rsnum=121912778
|variant=0003
}}{{ClinVar
|rsid=121912778
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=12704564
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TYRP1:7306
|GENE_NAME=TYRP1
|GENE_ID=7306
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.12704564C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=115501.0003
|CLNSIG=5
|CLNCUI=C1859932
|CLNDBN=Oculocutaneous albinism type 3
|Disease=Oculocutaneous albinism type 3
|CLNACC=RCV000019161.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1859932:203290:79433
}}