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rs794727372

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727372(A;A)
Make rs794727372(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position48465249
GeneRB1
is asnp
is mentioned by
dbSNPrs794727372
ebirs794727372
HLIrs794727372
Exacrs794727372
Varsomers794727372
Maprs794727372
PheGenIrs794727372
hapmaprs794727372
1000 genomesrs794727372
hgdprs794727372
ensemblrs794727372
gopubmedrs794727372
geneviewrs794727372
scholarrs794727372
googlers794727372
pharmgkbrs794727372
gwascentralrs794727372
openSNPrs794727372
23andMers794727372
23andMe allrs794727372
SNP Nexus

SNPshotrs794727372
SNPdbers794727372
MSV3drs794727372
GWAS Ctlgrs794727372
Max Magnitude0
ClinVar
Risk rs794727372(A;A)
Alt rs794727372(A;A)
Reference rs794727372(C;C)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49039385C>A
CLNSRC
CLNACC RCV000176364.1,