{{Rsnum
|rsid=121918166
|Gene=OCA2
|Chromosome=15
|position=27985101
|Orientation=plus
|GMAF=0.001837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=OCA2
}}{{omim
|id=611409
|rsnum=121918166
|variant=0004
}}{{ClinVar
|rsid=121918166
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=28230247
|CHROM=15
|GMAF=0.0018
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040416110100
|GENEINFO=OCA2:4948
|GENE_NAME=OCA2
|GENE_ID=4948
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.28230247C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=611409.0004
|CLNSIG=5
|CLNCUI=C0268495
|CLNDBN=Tyrosinase-positive oculocutaneous albinism
|Disease=Tyrosinase-positive oculocutaneous albinism
|CLNACC=RCV000001006.1
|Tags=RV;PM;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9982; 0.001837
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1232:C0268495:203200:79432:26336006
|COMMON=1
}}