{{Rsnum
|rsid=121918565
|Chromosome=6
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRPH2
|position=42722333
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRPH2
}}{{omim
|id=179605
|rsnum=121918565
|variant=0014
}}{{ClinVar
|rsid=121918565
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=42690071
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=PRPH2:5961
|GENE_NAME=PRPH2
|GENE_ID=5961
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.42690071A>G
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=179605.0014; RISN-RDS:c.2T>C
|CLNSIG=5
|CLNCUI=C1842914
|CLNDBN=Macular dystrophy, vitelliform, adult-onset; not provided
|Disease=Macular dystrophy; not provided
|CLNACC=RCV000014061.23; RCV000084961.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1842914:608161:99000
}}