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rs587778868

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778868(G;T)
Make rs587778868(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48463833
GeneRB1
is asnp
is mentioned by
dbSNPrs587778868
ebirs587778868
HLIrs587778868
Exacrs587778868
Varsomers587778868
Maprs587778868
PheGenIrs587778868
hapmaprs587778868
1000 genomesrs587778868
hgdprs587778868
ensemblrs587778868
gopubmedrs587778868
geneviewrs587778868
scholarrs587778868
googlers587778868
pharmgkbrs587778868
gwascentralrs587778868
openSNPrs587778868
23andMers587778868
23andMe allrs587778868
SNP Nexus

SNPshotrs587778868
SNPdbers587778868
MSV3drs587778868
GWAS Ctlgrs587778868
Max Magnitude0
ClinVar
Risk rs587778868(T;T)
Alt rs587778868(T;T)
Reference rs587778868(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49037969G>T
CLNSRC
CLNACC RCV000114690.1,