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rs587778850

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778850(A;A)
Make rs587778850(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48473391
GeneRB1
is asnp
is mentioned by
dbSNPrs587778850
ebirs587778850
HLIrs587778850
Exacrs587778850
Varsomers587778850
Maprs587778850
PheGenIrs587778850
hapmaprs587778850
1000 genomesrs587778850
hgdprs587778850
ensemblrs587778850
gopubmedrs587778850
geneviewrs587778850
scholarrs587778850
googlers587778850
pharmgkbrs587778850
gwascentralrs587778850
openSNPrs587778850
23andMers587778850
23andMe allrs587778850
SNP Nexus

SNPshotrs587778850
SNPdbers587778850
MSV3drs587778850
GWAS Ctlgrs587778850
Max Magnitude0
ClinVar
Risk rs587778850(A;A)
Alt rs587778850(A;A)
Reference rs587778850(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49047527G>A
CLNSRC
CLNACC RCV000114697.1,