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rs1060503087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503087(G;T)
Make rs1060503087(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position48379651
GeneRB1
is asnp
is mentioned by
dbSNPrs1060503087
dbSNP (old)rs1060503087
ClinGenrs1060503087
ebirs1060503087
HLIrs1060503087
Exacrs1060503087
Gnomadrs1060503087
Varsomers1060503087
LitVarrs1060503087
Maprs1060503087
PheGenIrs1060503087
Biobankrs1060503087
1000 genomesrs1060503087
hgdprs1060503087
ensemblrs1060503087
gopubmedrs1060503087
geneviewrs1060503087
scholarrs1060503087
googlers1060503087
pharmgkbrs1060503087
gwascentralrs1060503087
openSNPrs1060503087
23andMers1060503087
23andMe allrs1060503087
SNPshotrs1060503087
SNPdbers1060503087
MSV3drs1060503087
GWAS Ctlgrs1060503087
Max Magnitude0
ClinVar
Risk rs1060503087(T;T)
Alt rs1060503087(T;T)
Reference Rs1060503087(G;G)
Significance Probable-Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48953787G>T
CLNSRC
CLNACC RCV000462245.1,