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rs587776783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776783(A;A)
Make rs587776783(A;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position48373493
GeneRB1
is asnp
is mentioned by
dbSNPrs587776783
ebirs587776783
HLIrs587776783
Exacrs587776783
Varsomers587776783
Maprs587776783
PheGenIrs587776783
hapmaprs587776783
1000 genomesrs587776783
hgdprs587776783
ensemblrs587776783
gopubmedrs587776783
geneviewrs587776783
scholarrs587776783
googlers587776783
pharmgkbrs587776783
gwascentralrs587776783
openSNPrs587776783
23andMers587776783
23andMe allrs587776783
SNP Nexus

SNPshotrs587776783
SNPdbers587776783
MSV3drs587776783
GWAS Ctlgrs587776783
Max Magnitude0
ClinVar
Risk rs587776783(A;A)
Alt rs587776783(A;A)
Reference rs587776783(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48947629G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000114724.5,