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rs121913303

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913303(C;T)
Make rs121913303(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48381402
GeneRB1
is asnp
is mentioned by
dbSNPrs121913303
ebirs121913303
HLIrs121913303
Exacrs121913303
Varsomers121913303
Maprs121913303
PheGenIrs121913303
hapmaprs121913303
1000 genomesrs121913303
hgdprs121913303
ensemblrs121913303
gopubmedrs121913303
geneviewrs121913303
scholarrs121913303
googlers121913303
pharmgkbrs121913303
gwascentralrs121913303
openSNPrs121913303
23andMers121913303
23andMe allrs121913303
SNP Nexus

SNPshotrs121913303
SNPdbers121913303
MSV3drs121913303
GWAS Ctlgrs121913303
Max Magnitude0
ClinVar
Risk rs121913303(T;T)
Alt rs121913303(T;T)
Reference rs121913303(C;C)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48955538C>T
CLNSRC
CLNACC RCV000114733.1,