Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853947

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853947(G;G)
Make rs878853947(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position48373431
GeneRB1
is asnp
is mentioned by
dbSNPrs878853947
ebirs878853947
HLIrs878853947
Exacrs878853947
Varsomers878853947
Maprs878853947
PheGenIrs878853947
hapmaprs878853947
1000 genomesrs878853947
hgdprs878853947
ensemblrs878853947
gopubmedrs878853947
geneviewrs878853947
scholarrs878853947
googlers878853947
pharmgkbrs878853947
gwascentralrs878853947
openSNPrs878853947
23andMers878853947
23andMe allrs878853947
SNP Nexus

SNPshotrs878853947
SNPdbers878853947
MSV3drs878853947
GWAS Ctlgrs878853947
Max Magnitude0
ClinVar
Risk rs878853947(G;G)
Alt rs878853947(G;G)
Reference rs878853947(T;T)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48947567T>G
CLNSRC
CLNACC RCV000226485.1,