{{Rsnum
|rsid=4961206
|Gene=CNGB3
|Chromosome=8
|position=86654023
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=C
|GMAF=0.3421
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=CNGB3
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 42.5 | 43.4 | 14.2
| HCB | 66.2 | 29.4 | 4.4
| JPT | 72.6 | 23.9 | 3.5
| YRI | 27.9 | 57.1 | 15.0
| ASW | 38.6 | 47.4 | 14.0
| CHB | 66.2 | 29.4 | 4.4
| CHD | 75.9 | 22.2 | 1.9
| GIH | 52.5 | 40.6 | 6.9
| LWK | 33.0 | 45.9 | 21.1
| MEX | 29.3 | 55.2 | 15.5
| MKK | 36.5 | 51.3 | 12.2
| TSI | 38.2 | 53.9 | 7.8
| HapMapRevision=28
}}

{{Venter SNP
|rsid=4961206
|allele=G
|frequency=0.367
|uid=1103652373235
|type=heterozygous_SNP
|hugo=CNGB3
|ensembl gene=ENSG00000170289
|ensembl transcript=ENST00000320005
|sift=TOLERATED
|disease=Defects in CNGB3 are a cause of achromatopsia 3 (ACHM3) (MIM:262300); also known as Pingelapese blindness. ACHM3 is a congenital complete achromatopsia and is distinct from total colorblindness mainly because of the consistent concurrence of severe myopia.
}}

{{GET Evidence
|gene=CNGB3
|aa_change=Thr298Pro
|aa_change_short=T298P
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4961206
|overall_frequency_n=6911
|overall_frequency_d=10752
|overall_frequency=0.642764
|n_genomes=52
|n_genomes_annotated=0
|n_haplomes=69
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=3
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|pph2_score=0.007
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=4
|autoscore=3
|n_web_uneval=5
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}