{{Rsnum
|rsid = 3092891
|Gene = RB1
|Orientation=plus
|ReferenceAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=13
|position=48379594
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RB1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=RETINOBLASTOMA
|id=180200
|rsnum=3092891
|variant=0003
}}

{{ClinVar
|rsid=3092891
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=48953730
|CHROM=13
|dbSNPBuildID=103
|SSR=0
|SAO=1
|VP=0x050268000000040103110100
|GENEINFO=RB1:5925
|GENE_NAME=RB1
|GENE_ID=5925
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.48953730C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=614041.0003
|CLNSIG=5
|CLNCUI=C0035335
|CLNDBN=Retinoblastoma
|Disease=Retinoblastoma
|CLNACC=RCV000013946.1
|Tags=PM;PMC;S3D;VLD;GNO;OTHERKG;PH3;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1452:C0035335:180200:790
}}

{{PMID Auto
|PMID=18852891
|Title=Distribution and effects of nonsense polymorphisms in human genes.
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}