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rs587778854

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778854(-;-)
Make rs587778854(-;T)
Make rs587778854(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48345162
GeneRB1
is asnp
is mentioned by
dbSNPrs587778854
ebirs587778854
HLIrs587778854
Exacrs587778854
Varsomers587778854
Maprs587778854
PheGenIrs587778854
hapmaprs587778854
1000 genomesrs587778854
hgdprs587778854
ensemblrs587778854
gopubmedrs587778854
geneviewrs587778854
scholarrs587778854
googlers587778854
pharmgkbrs587778854
gwascentralrs587778854
openSNPrs587778854
23andMers587778854
23andMe allrs587778854
SNP Nexus

SNPshotrs587778854
SNPdbers587778854
MSV3drs587778854
GWAS Ctlgrs587778854
Max Magnitude0
ClinVar
Risk rs587778854(T;T)
Alt rs587778854(T;T)
Reference rs587778854(;)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48919298dupT
CLNSRC
CLNACC RCV000114705.1,