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rs121913305

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913305(C;T)
Make rs121913305(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48453032
GeneRB1
is asnp
is mentioned by
dbSNPrs121913305
ebirs121913305
HLIrs121913305
Exacrs121913305
Varsomers121913305
Maprs121913305
PheGenIrs121913305
hapmaprs121913305
1000 genomesrs121913305
hgdprs121913305
ensemblrs121913305
gopubmedrs121913305
geneviewrs121913305
scholarrs121913305
googlers121913305
pharmgkbrs121913305
gwascentralrs121913305
openSNPrs121913305
23andMers121913305
23andMe allrs121913305
SNP Nexus

SNPshotrs121913305
SNPdbers121913305
MSV3drs121913305
GWAS Ctlgrs121913305
Max Magnitude0
ClinVar
Risk rs121913305(T;T)
Alt rs121913305(T;T)
Reference rs121913305(C;C)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49027168C>T
CLNSRC
CLNACC RCV000114677.1,