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rs587778833

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778833(C;T)
Make rs587778833(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48456298
GeneRB1
is asnp
is mentioned by
dbSNPrs587778833
ebirs587778833
HLIrs587778833
Exacrs587778833
Varsomers587778833
Maprs587778833
PheGenIrs587778833
hapmaprs587778833
1000 genomesrs587778833
hgdprs587778833
ensemblrs587778833
gopubmedrs587778833
geneviewrs587778833
scholarrs587778833
googlers587778833
pharmgkbrs587778833
gwascentralrs587778833
openSNPrs587778833
23andMers587778833
23andMe allrs587778833
SNP Nexus

SNPshotrs587778833
SNPdbers587778833
MSV3drs587778833
GWAS Ctlgrs587778833
Max Magnitude0
ClinVar
Risk rs587778833(T;T)
Alt rs587778833(T;T)
Reference rs587778833(C;C)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49030434C>T
CLNSRC
CLNACC RCV000114680.1,