{{Rsnum
|rsid=121918285
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=BEST1
|position=61951893
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=BEST1
}}{{omim
|id=607854
|rsnum=121918285
|variant=0014
}}{{ClinVar
|rsid=121918285
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=61719365
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=BEST1:7439
|GENE_NAME=BEST1
|GENE_ID=7439
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.61719365C>G; NC_000011.9:g.61719365C>T
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=607854.0014; RISN-VMD2:c.87C>T
|CLNSIG=5
|CLNCUI=C0339510
|CLNDBN=Vitelliform dystrophy; not provided
|Disease=Vitelliform dystrophy; not provided
|CLNACC=RCV000002849.1; RCV000086177.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1167:C0339510:153700:1243:90036004
}}