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rs121913302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913302(C;T)
Make rs121913302(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48379624
GeneRB1
is asnp
is mentioned by
dbSNPrs121913302
dbSNP (old)rs121913302
ClinGenrs121913302
ebirs121913302
HLIrs121913302
Exacrs121913302
Gnomadrs121913302
Varsomers121913302
Maprs121913302
PheGenIrs121913302
Biobankrs121913302
1000 genomesrs121913302
hgdprs121913302
ensemblrs121913302
gopubmedrs121913302
geneviewrs121913302
scholarrs121913302
googlers121913302
pharmgkbrs121913302
gwascentralrs121913302
openSNPrs121913302
23andMers121913302
23andMe allrs121913302
SNP Nexus

SNPshotrs121913302
SNPdbers121913302
MSV3drs121913302
GWAS Ctlgrs121913302
Max Magnitude0
ClinVar
Risk rs121913302(T;T)
Alt rs121913302(T;T)
Reference Rs121913302(C;C)
Significance Other
Disease Retinoblastoma not provided Hereditary cancer-predisposing syndrome
Variation info
Gene RB1
CLNDBN Retinoblastoma not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.48953760C>T
CLNSRC
CLNACC RCV000114729.2, RCV000486601.1, RCV000492246.1,