{{Rsnum
|rsid=137853290
|Chromosome=15
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RLBP1
|position=89215133
|Gene_s=RLBP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=180090
|variant=0001
|rsnum=137853290
}}{{ClinVar
|rsid=137853290
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=89758364
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RLBP1:6017
|GENE_NAME=RLBP1
|GENE_ID=6017
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.89758364C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=180090.0001
|CLNSIG=5
|CLNCUI=C0311338
|CLNDBN=Pigmentary retinal dystrophy; Retinitis punctata albescens
|Disease=Pigmentary retinal dystrophy; Retinitis punctata albescens
|CLNACC=RCV000013973.23; RCV000013974.23
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=C0311338:136880:227796:52427:68222009; C1405854
}}