{{Rsnum
|rsid=137853138
|Gene=CRB1
|Chromosome=1
|position=197328835
|Orientation=plus
|GMAF=0.002296
|Gene_s=CRB1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{omim
|id=604210
|variant=0010
|rsnum=137853138
}}{{ClinVar
|rsid=137853138
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=197328835
|CHROM=1
|GMAF=0.0023
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260080a05040416110100
|GENEINFO=CRB1:23418
|GENE_NAME=CRB1
|GENE_ID=23418
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.197328835G>A
|CLNSRC=ClinVar; Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_201253.2:c.484G>A; NR_047563.1:n.693G>A; 13677; 604210.0010
|CLNSIG=5
|CLNCUI=C1868310
|CLNDBN=Pigmented paravenous chorioretinal atrophy; not provided
|Disease=Pigmented paravenous chorioretinal atrophy; not provided
|CLNACC=RCV000006092.1; RCV000082821.1
|Tags=PM;S3D;NSM;REF;INT;ASP;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9977; 0.002296
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1868310:172870:ORPHA251295
|COMMON=1
}}