{{Rsnum
|rsid=104894130
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TYRP1
|position=12695626
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
}}{{omim
|id=115501
|rsnum=104894130
|variant=0002
}}{{ClinVar
|rsid=104894130
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=12695626
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=TYRP1:7306
|GENE_NAME=TYRP1
|GENE_ID=7306
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.12695626C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=115501.0002
|CLNSIG=5
|CLNCUI=C1859932
|CLNDBN=Oculocutaneous albinism type 3; ALBINISM, OCULOCUTANEOUS, TYPE II, MODIFIER OF
|Disease=Oculocutaneous albinism type 3; ALBINISM
|CLNACC=RCV000019159.22; RCV000019160.22
|Tags=PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1859932:203290:79433
}}