{{Rsnum
|rsid=61755792
|Chromosome=6
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRPH2
|position=42721821
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRPH2
}}{{omim
|id=179605
|rsnum=61755792
|variant=0007
}}

{{ClinVar
|rsid=61755792
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=42689559
|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.42689559G>A; NC_000006.11:g.42689559G>C
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=179605.0007; RISN-RDS:c.514C>T; RISN-RDS:c.514C>G
|CLNSIG=5
|CLNCUI=C2751290
|CLNDBN=Choroidal dystrophy, central areolar 2; not provided
|Disease=Choroidal dystrophy; not provided
|CLNACC=RCV000014056.23; RCV000084981.1; RCV000084980.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2751290:613105:75377
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}