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rs587778865

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778865(A;A)
Make rs587778865(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48456314
GeneRB1
is asnp
is mentioned by
dbSNPrs587778865
ebirs587778865
HLIrs587778865
Exacrs587778865
Varsomers587778865
Maprs587778865
PheGenIrs587778865
hapmaprs587778865
1000 genomesrs587778865
hgdprs587778865
ensemblrs587778865
gopubmedrs587778865
geneviewrs587778865
scholarrs587778865
googlers587778865
pharmgkbrs587778865
gwascentralrs587778865
openSNPrs587778865
23andMers587778865
23andMe allrs587778865
SNP Nexus

SNPshotrs587778865
SNPdbers587778865
MSV3drs587778865
GWAS Ctlgrs587778865
Max Magnitude0
ClinVar
Risk rs587778865(A;A)
Alt rs587778865(A;A)
Reference rs587778865(T;T)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49030450T>A
CLNSRC
CLNACC RCV000114681.1,