{{Rsnum
|rsid=121918289
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=BEST1
|position=61955726
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=BEST1
}}{{omim
|id=607854
|rsnum=121918289
|variant=0019
}}{{ClinVar
|rsid=121918289
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=61723198
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=BEST1:7439
|GENE_NAME=BEST1
|GENE_ID=7439
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.61723198G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607854.0019
|CLNSIG=5
|CLNCUI=C1860406
|CLNDBN=Vitreoretinochoroidopathy dominant
|Disease=Vitreoretinochoroidopathy dominant
|CLNACC=RCV000002867.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1860406:193220:263347:3086
}}