{{Rsnum
|rsid=10902758
|Gene=PDE6B
|Chromosome=4
|position=654854
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.0005
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TGM5
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 0.0
| HCB | 0.0 | 0.0 | 0.0
| JPT | 0.0 | 0.0 | 0.0
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 96.8 | 3.2 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=10902758
|allele=A
|frequency=
|uid=1103654313193
|type=homozygous_SNP
|hugo=PDE6B
|ensembl gene=ENSG00000133256
|ensembl transcript=ENST00000255622
|sift=TOLERATED
|disease=Defects in PDE6B are a cause of autosomal dominant congenital stationary night blindness (CSNB3) (MIM:163500).
}}

{{PMID Auto
|PMID=19339744
|Title=Genetic analysis of Indian families with autosomal recessive retinitis pigmentosa by homozygosity screening.
|OA=1
}}

{{GET Evidence
|gene=PDE6B
|aa_change=Val41Ile
|aa_change_short=V41I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10902758
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|genetests_testable=Y
|nblosum100=-4
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}