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rs587778864

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778864(C;T)
Make rs587778864(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48453020
GeneRB1
is asnp
is mentioned by
dbSNPrs587778864
ebirs587778864
HLIrs587778864
Exacrs587778864
Varsomers587778864
Maprs587778864
PheGenIrs587778864
hapmaprs587778864
1000 genomesrs587778864
hgdprs587778864
ensemblrs587778864
gopubmedrs587778864
geneviewrs587778864
scholarrs587778864
googlers587778864
pharmgkbrs587778864
gwascentralrs587778864
openSNPrs587778864
23andMers587778864
23andMe allrs587778864
SNP Nexus

SNPshotrs587778864
SNPdbers587778864
MSV3drs587778864
GWAS Ctlgrs587778864
Max Magnitude0
ClinVar
Risk rs587778864(T;T)
Alt rs587778864(T;T)
Reference rs587778864(C;C)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49027156C>T
CLNSRC
CLNACC RCV000114676.1,