{{Rsnum
|rsid=387907171
|Chromosome=9
|position=12694273
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TYRP1
|Gene_s=TYRP1
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=T
|CHROM=9
|CLNACC=RCV000024318.26
|CLNALLE=1
|CLNDBN=Skin/hair/eye pigmentation, variation in, 11
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2677086:612271
|CLNHGVS=NC_000009.11:g.12694273C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=115501.0007
|Disease=Skin/hair/eye pigmentation
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=12694273
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907171
|GENEINFO=TYRP1:7306
|GENE_ID=7306
|GENE_NAME=TYRP1
}}