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rs587778851

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778851(-;-)
Make rs587778851(-;C)
Make rs587778851(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48476705
GeneRB1
is asnp
is mentioned by
dbSNPrs587778851
ebirs587778851
HLIrs587778851
Exacrs587778851
Varsomers587778851
Maprs587778851
PheGenIrs587778851
hapmaprs587778851
1000 genomesrs587778851
hgdprs587778851
ensemblrs587778851
gopubmedrs587778851
geneviewrs587778851
scholarrs587778851
googlers587778851
pharmgkbrs587778851
gwascentralrs587778851
openSNPrs587778851
23andMers587778851
23andMe allrs587778851
SNP Nexus

SNPshotrs587778851
SNPdbers587778851
MSV3drs587778851
GWAS Ctlgrs587778851
Max Magnitude0
ClinVar
Risk rs587778851(C;C)
Alt rs587778851(C;C)
Reference rs587778851(;)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49050841dupC
CLNSRC
CLNACC RCV000114698.1,