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rs587776780

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776780(C;C)
Make rs587776780(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48456351
GeneRB1
is asnp
is mentioned by
dbSNPrs587776780
ebirs587776780
HLIrs587776780
Exacrs587776780
Varsomers587776780
Maprs587776780
PheGenIrs587776780
hapmaprs587776780
1000 genomesrs587776780
hgdprs587776780
ensemblrs587776780
gopubmedrs587776780
geneviewrs587776780
scholarrs587776780
googlers587776780
pharmgkbrs587776780
gwascentralrs587776780
openSNPrs587776780
23andMers587776780
23andMe allrs587776780
SNP Nexus

SNPshotrs587776780
SNPdbers587776780
MSV3drs587776780
GWAS Ctlgrs587776780
Max Magnitude0
ClinVar
Risk rs587776780(C;C)
Alt rs587776780(C;C)
Reference rs587776780(T;T)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49030487T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013945.4,