{{Rsnum
|rsid=121918582
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PDE6B
|position=653912
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PDE6B,TGM5
}}{{omim
|id=180072
|rsnum=121918582
|variant=0005
}}{{ClinVar
|rsid=121918582
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=647701
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PDE6B:5158
|GENE_NAME=PDE6B
|GENE_ID=5158
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.647701C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=180072.0005
|CLNSIG=5
|CLNCUI=C1876182
|CLNDBN=Congenital stationary night blindness, autosomal dominant 2
|Disease=Congenital stationary night blindness
|CLNACC=RCV000013986.22
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1876182:163500:215
}}