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rs794727481

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727481(A;A)
Make rs794727481(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position48342631
GeneRB1
is asnp
is mentioned by
dbSNPrs794727481
ebirs794727481
HLIrs794727481
Exacrs794727481
Varsomers794727481
Maprs794727481
PheGenIrs794727481
hapmaprs794727481
1000 genomesrs794727481
hgdprs794727481
ensemblrs794727481
gopubmedrs794727481
geneviewrs794727481
scholarrs794727481
googlers794727481
pharmgkbrs794727481
gwascentralrs794727481
openSNPrs794727481
23andMers794727481
23andMe allrs794727481
SNP Nexus

SNPshotrs794727481
SNPdbers794727481
MSV3drs794727481
GWAS Ctlgrs794727481
Max Magnitude0
ClinVar
Risk rs794727481(A;A)
Alt rs794727481(A;A)
Reference rs794727481(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48916767G>A
CLNSRC
CLNACC RCV000177038.1,