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rs1060503088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060503088(G;G)
Make rs1060503088(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position48452981
GeneRB1
is asnp
is mentioned by
dbSNPrs1060503088
dbSNP (old)rs1060503088
ClinGenrs1060503088
ebirs1060503088
HLIrs1060503088
Exacrs1060503088
Gnomadrs1060503088
Varsomers1060503088
Maprs1060503088
PheGenIrs1060503088
Biobankrs1060503088
1000 genomesrs1060503088
hgdprs1060503088
ensemblrs1060503088
gopubmedrs1060503088
geneviewrs1060503088
scholarrs1060503088
googlers1060503088
pharmgkbrs1060503088
gwascentralrs1060503088
openSNPrs1060503088
23andMers1060503088
23andMe allrs1060503088
SNPshotrs1060503088
SNPdbers1060503088
MSV3drs1060503088
GWAS Ctlgrs1060503088
Max Magnitude0
ClinVar
Risk rs1060503088(G;G)
Alt rs1060503088(G;G)
Reference Rs1060503088(T;T)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49027117T>G
CLNSRC
CLNACC RCV000471747.1,