{{Rsnum
|rsid=121918567
|Gene=PRPH2
|Chromosome=6
|position=42704609
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=LOC101929618,PRPH2
}}{{omim
|id=179605
|rsnum=121918567
|variant=0021
}}{{ClinVar
|rsid=121918567
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=42672347
|CHROM=6
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000016110100
|GENEINFO=PRPH2:5961
|GENE_NAME=PRPH2
|GENE_ID=5961
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.42672347C>A
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=179605.0021; RISN-RDS:c.584G>T
|CLNSIG=5
|CLNCUI=C2751290
|CLNDBN=Choroidal dystrophy, central areolar 2; not provided
|Disease=Choroidal dystrophy; not provided
|CLNACC=RCV000014070.23; RCV000084990.1
|Tags=RV;PM;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2751290:613105:75377
|COMMON=0
}}