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rs587778841

From SNPedia

Orientationplus
Geno Mag Summary
(TGCT;TGCT) 0 common in clinvar
Make rs587778841(-;-)
Make rs587778841(-;TGCT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48345137
GeneRB1
is asnp
is mentioned by
dbSNPrs587778841
ebirs587778841
HLIrs587778841
Exacrs587778841
Varsomers587778841
Maprs587778841
PheGenIrs587778841
hapmaprs587778841
1000 genomesrs587778841
hgdprs587778841
ensemblrs587778841
gopubmedrs587778841
geneviewrs587778841
scholarrs587778841
googlers587778841
pharmgkbrs587778841
gwascentralrs587778841
openSNPrs587778841
23andMers587778841
23andMe allrs587778841
SNP Nexus

SNPshotrs587778841
SNPdbers587778841
MSV3drs587778841
GWAS Ctlgrs587778841
Max Magnitude0
ClinVar
Risk rs587778841(;)
Alt rs587778841(;)
Reference rs587778841(TGCT;TGCT)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48919273_48919276delTGCT
CLNSRC
CLNACC RCV000114703.1,