Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060503077

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503077(G;T)
Make rs1060503077(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position48367521
GeneRB1
is asnp
is mentioned by
dbSNPrs1060503077
dbSNP (old)rs1060503077
ClinGenrs1060503077
ebirs1060503077
HLIrs1060503077
Exacrs1060503077
Gnomadrs1060503077
Varsomers1060503077
Maprs1060503077
PheGenIrs1060503077
Biobankrs1060503077
1000 genomesrs1060503077
hgdprs1060503077
ensemblrs1060503077
gopubmedrs1060503077
geneviewrs1060503077
scholarrs1060503077
googlers1060503077
pharmgkbrs1060503077
gwascentralrs1060503077
openSNPrs1060503077
23andMers1060503077
23andMe allrs1060503077
SNPshotrs1060503077
SNPdbers1060503077
MSV3drs1060503077
GWAS Ctlgrs1060503077
Max Magnitude0
ClinVar
Risk rs1060503077(T;T)
Alt rs1060503077(T;T)
Reference Rs1060503077(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48941657G>T
CLNSRC
CLNACC RCV000471380.1,