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rs587778835

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778835(C;T)
Make rs587778835(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48463821
GeneRB1
is asnp
is mentioned by
dbSNPrs587778835
ebirs587778835
HLIrs587778835
Exacrs587778835
Varsomers587778835
Maprs587778835
PheGenIrs587778835
hapmaprs587778835
1000 genomesrs587778835
hgdprs587778835
ensemblrs587778835
gopubmedrs587778835
geneviewrs587778835
scholarrs587778835
googlers587778835
pharmgkbrs587778835
gwascentralrs587778835
openSNPrs587778835
23andMers587778835
23andMe allrs587778835
SNP Nexus

SNPshotrs587778835
SNPdbers587778835
MSV3drs587778835
GWAS Ctlgrs587778835
Max Magnitude0
ClinVar
Risk rs587778835(T;T)
Alt rs587778835(T;T)
Reference rs587778835(C;C)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49037957C>T
CLNSRC
CLNACC RCV000114689.1,