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rs1060503074

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060503074(G;G)
Make rs1060503074(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position48373494
GeneRB1
is asnp
is mentioned by
dbSNPrs1060503074
dbSNP (old)rs1060503074
ClinGenrs1060503074
ebirs1060503074
HLIrs1060503074
Exacrs1060503074
Gnomadrs1060503074
Varsomers1060503074
LitVarrs1060503074
Maprs1060503074
PheGenIrs1060503074
Biobankrs1060503074
1000 genomesrs1060503074
hgdprs1060503074
ensemblrs1060503074
gopubmedrs1060503074
geneviewrs1060503074
scholarrs1060503074
googlers1060503074
pharmgkbrs1060503074
gwascentralrs1060503074
openSNPrs1060503074
23andMers1060503074
23andMe allrs1060503074
SNPshotrs1060503074
SNPdbers1060503074
MSV3drs1060503074
GWAS Ctlgrs1060503074
Max Magnitude0
ClinVar
Risk rs1060503074(G;G)
Alt rs1060503074(G;G)
Reference Rs1060503074(T;T)
Significance Probable-Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48947630T>G
CLNSRC
CLNACC RCV000469761.1,