{{Rsnum
|rsid=35365413
|Gene=CNGB3
|Chromosome=8
|position=86628994
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CNGB3
}}Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.{{PMID|15712225}}
{{omim
|id=605080
|rsnum=35365413
|variant=0006
}}

{{ClinVar
|rsid=35365413
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=87641222
|CHROM=8
|GMAF=0.0014
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050360000000040516110100
|GENEINFO=CNGB3:54714
|GENE_NAME=CNGB3
|GENE_ID=54714
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.87641222A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605080.0006
|CLNSIG=5
|CLNCUI=C1855465
|CLNDBN=Stargardt disease 1
|Disease=Stargardt disease 1
|CLNACC=RCV000005538.1
|Tags=PM;S3D;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1855465:248200:827
|COMMON=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}