{{Rsnum
|rsid=61755798
|Chromosome=6
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PRPH2
|position=42704564
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC101929618,PRPH2
}}{{omim
|id=179605
|rsnum=61755798
|variant=0012
}}{{ClinVar
|rsid=61755798
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=42672302
|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; 2
|CLNHGVS=NC_000006.11:g.42672302G>A; NC_000006.11:g.42672302G>C
|CLNSRC=Retina International; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=RISN-RDS:c.629C>T; 179605.0012; RISN-RDS:c.629C>G
|CLNSIG=5
|CLNCUI=C1842914
|CLNDBN=not provided; Macular dystrophy, vitelliform, adult-onset
|Disease=not provided; Macular dystrophy
|CLNACC=RCV000084998.1; RCV000014059.23; RCV000084997.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1842914:608161:99000
}}