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rs587778858

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778858(G;T)
Make rs587778858(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48453035
GeneRB1
is asnp
is mentioned by
dbSNPrs587778858
ebirs587778858
HLIrs587778858
Exacrs587778858
Varsomers587778858
Maprs587778858
PheGenIrs587778858
hapmaprs587778858
1000 genomesrs587778858
hgdprs587778858
ensemblrs587778858
gopubmedrs587778858
geneviewrs587778858
scholarrs587778858
googlers587778858
pharmgkbrs587778858
gwascentralrs587778858
openSNPrs587778858
23andMers587778858
23andMe allrs587778858
SNP Nexus

SNPshotrs587778858
SNPdbers587778858
MSV3drs587778858
GWAS Ctlgrs587778858
Max Magnitude0
ClinVar
Risk rs587778858(T;T)
Alt rs587778858(T;T)
Reference rs587778858(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49027171G>T
CLNSRC
CLNACC RCV000114678.1,