{{Rsnum
|rsid=267606677
|Chromosome=11
|position=61957430
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=BEST1
|Gene_s=BEST1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000002873.1; RCV000002874.1; RCV000086158.1
|CLNALLE=1
|CLNDBN=Vitelliform dystrophy; Retinitis pigmentosa, concentric; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1167:C0339510:153700:1243:90036004; C2750789
|CLNHGVS=NC_000011.9:g.61724902A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNSRCID=607854.0024; RISN-VMD2:c.680A>G
|Disease=Vitelliform dystrophy; Retinitis pigmentosa; not provided
|FwdALT=G
|FwdREF=A
|GENEINFO=BEST1:7439
|GENE_ID=7439
|GENE_NAME=BEST1
|REF=A
|RSPOS=61724902
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050160000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606677
}}