{{Rsnum
|rsid=397515360
|Chromosome=8
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=CNGB3
|position=86643781
|Gene_s=CNGB3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=8
|CLNACC=RCV000005535.2; RCV000005536.1; RCV000081978.1
|CLNALLE=1
|CLNDBN=Achromatopsia 3; Stargardt disease 1; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1418:C1849792:262300:49382; C1855465:248200:827
|CLNHGVS=NC_000008.10:g.87656009delG
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1418; 605080.0002
|Disease=Achromatopsia 3; Stargardt disease 1; not provided
|FwdREF=C
|GENEINFO=CNGB3:54714
|GENE_ID=54714
|GENE_NAME=CNGB3
|REF=AG
|RSPOS=87656008
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397515360
}}