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rs794727199

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727199(A;A)
Make rs794727199(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position48452992
GeneRB1
is asnp
is mentioned by
dbSNPrs794727199
ebirs794727199
HLIrs794727199
Exacrs794727199
Varsomers794727199
Maprs794727199
PheGenIrs794727199
hapmaprs794727199
1000 genomesrs794727199
hgdprs794727199
ensemblrs794727199
gopubmedrs794727199
geneviewrs794727199
scholarrs794727199
googlers794727199
pharmgkbrs794727199
gwascentralrs794727199
openSNPrs794727199
23andMers794727199
23andMe allrs794727199
SNP Nexus

SNPshotrs794727199
SNPdbers794727199
MSV3drs794727199
GWAS Ctlgrs794727199
Max Magnitude0
ClinVar
Risk rs794727199(A;A)
Alt rs794727199(A;A)
Reference rs794727199(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49027128G>A
CLNSRC
CLNACC RCV000175271.1,