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rs587778847

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778847(G;T)
Make rs587778847(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48379607
GeneRB1
is asnp
is mentioned by
dbSNPrs587778847
ebirs587778847
HLIrs587778847
Exacrs587778847
Varsomers587778847
Maprs587778847
PheGenIrs587778847
hapmaprs587778847
1000 genomesrs587778847
hgdprs587778847
ensemblrs587778847
gopubmedrs587778847
geneviewrs587778847
scholarrs587778847
googlers587778847
pharmgkbrs587778847
gwascentralrs587778847
openSNPrs587778847
23andMers587778847
23andMe allrs587778847
SNP Nexus

SNPshotrs587778847
SNPdbers587778847
MSV3drs587778847
GWAS Ctlgrs587778847
Max Magnitude0
ClinVar
Risk rs587778847(T;T)
Alt rs587778847(T;T)
Reference rs587778847(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48953743G>T
CLNSRC
CLNACC RCV000114728.1,