{{Rsnum
|rsid=281865424
|Chromosome=9
|position=12702424
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TYRP1
|Gene_s=TYRP1
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|Orientation=plus
}}{{ClinVar
|ALT=A
|CHROM=9
|CLNACC=RCV000019162.26
|CLNALLE=1
|CLNDBN=Oculocutaneous albinism type 3
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1859932:203290:79433
|CLNHGVS=NC_000009.11:g.12702424G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=115501.0004
|Disease=Oculocutaneous albinism type 3
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=12702424
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=281865424
|GENEINFO=TYRP1:7306
|GENE_ID=7306
|GENE_NAME=TYRP1
}}