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

rs121913298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913298(A;A)
Make rs121913298(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position48349012
GeneRB1
is asnp
is mentioned by
dbSNPrs121913298
dbSNP (old)rs121913298
ClinGenrs121913298
ebirs121913298
HLIrs121913298
Exacrs121913298
Gnomadrs121913298
Varsomers121913298
LitVarrs121913298
Maprs121913298
PheGenIrs121913298
Biobankrs121913298
1000 genomesrs121913298
hgdprs121913298
ensemblrs121913298
gopubmedrs121913298
geneviewrs121913298
scholarrs121913298
googlers121913298
pharmgkbrs121913298
gwascentralrs121913298
openSNPrs121913298
23andMers121913298
23andMe allrs121913298
SNPshotrs121913298
SNPdbers121913298
MSV3drs121913298
GWAS Ctlgrs121913298
Max Magnitude0
ClinVar
Risk rs121913298(A;A)
Alt rs121913298(A;A)
Reference Rs121913298(T;T)
Significance Probable-Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48923148T>A
CLNSRC
CLNACC RCV000437633.1,