{{Rsnum
|rsid=121909835
|Chromosome=5
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PDE6A
|position=149883511
|Gene_s=PDE6A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=5
|CLNACC=RCV000022755.23
|CLNALLE=1
|CLNDBN=Retinitis pigmentosa 43
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1417:C3151139:613810:791
|CLNHGVS=NC_000005.9:g.149263074C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=180071.0004
|Disease=Retinitis pigmentosa 43
|FwdALT=A
|FwdREF=G
|GENEINFO=PDE6A:5145
|GENE_ID=5145
|GENE_NAME=PDE6A
|REF=C
|RSPOS=149263074
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|VC=SNV
|VP=0x050268000000000002100100
|WGT=0
|dbSNPBuildID=133
|rsid=121909835
}}{{PMID Auto
|PMID=21039428
|Title=Identification of a novel mutation in the human PDE6A gene in autosomal recessive retinitis pigmentosa: homology with the nmf28/nmf28 mice model.
}}