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

rs121913296

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913296(G;T)
Make rs121913296(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48345108
GeneRB1
is asnp
is mentioned by
dbSNPrs121913296
ebirs121913296
HLIrs121913296
Exacrs121913296
Varsomers121913296
Maprs121913296
PheGenIrs121913296
hapmaprs121913296
1000 genomesrs121913296
hgdprs121913296
ensemblrs121913296
gopubmedrs121913296
geneviewrs121913296
scholarrs121913296
googlers121913296
pharmgkbrs121913296
gwascentralrs121913296
openSNPrs121913296
23andMers121913296
23andMe allrs121913296
SNP Nexus

SNPshotrs121913296
SNPdbers121913296
MSV3drs121913296
GWAS Ctlgrs121913296
Max Magnitude0
ClinVar
Risk rs121913296(T;T)
Alt rs121913296(T;T)
Reference rs121913296(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48919244G>T
CLNSRC
CLNACC RCV000114702.1,