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rs121913304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913304(C;T)
Make rs121913304(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position48381414
GeneRB1
is asnp
is mentioned by
dbSNPrs121913304
ebirs121913304
HLIrs121913304
Exacrs121913304
Varsomers121913304
Maprs121913304
PheGenIrs121913304
hapmaprs121913304
1000 genomesrs121913304
hgdprs121913304
ensemblrs121913304
gopubmedrs121913304
geneviewrs121913304
scholarrs121913304
googlers121913304
pharmgkbrs121913304
gwascentralrs121913304
openSNPrs121913304
23andMers121913304
23andMe allrs121913304
SNP Nexus

SNPshotrs121913304
SNPdbers121913304
MSV3drs121913304
GWAS Ctlgrs121913304
Max Magnitude0
OMIM180200
Desc
Variant0022
Relatedalso
ClinVar
Risk rs121913304(T;T)
Alt rs121913304(T;T)
Reference rs121913304(C;C)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma, trilateral Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48955550C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013966.2, RCV000114734.1,