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rs587778848

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778848(C;C)
Make rs587778848(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48380215
GeneRB1
is asnp
is mentioned by
dbSNPrs587778848
ebirs587778848
HLIrs587778848
Exacrs587778848
Varsomers587778848
Maprs587778848
PheGenIrs587778848
hapmaprs587778848
1000 genomesrs587778848
hgdprs587778848
ensemblrs587778848
gopubmedrs587778848
geneviewrs587778848
scholarrs587778848
googlers587778848
pharmgkbrs587778848
gwascentralrs587778848
openSNPrs587778848
23andMers587778848
23andMe allrs587778848
SNP Nexus

SNPshotrs587778848
SNPdbers587778848
MSV3drs587778848
GWAS Ctlgrs587778848
Max Magnitude0
ClinVar
Risk rs587778848(C;C)
Alt rs587778848(C;C)
Reference rs587778848(T;T)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48954351T>C
CLNSRC
CLNACC RCV000114732.1,