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rs587778855

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778855(A;T)
Make rs587778855(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48367575
GeneRB1
is asnp
is mentioned by
dbSNPrs587778855
ebirs587778855
HLIrs587778855
Exacrs587778855
Varsomers587778855
Maprs587778855
PheGenIrs587778855
hapmaprs587778855
1000 genomesrs587778855
hgdprs587778855
ensemblrs587778855
gopubmedrs587778855
geneviewrs587778855
scholarrs587778855
googlers587778855
pharmgkbrs587778855
gwascentralrs587778855
openSNPrs587778855
23andMers587778855
23andMe allrs587778855
SNP Nexus

SNPshotrs587778855
SNPdbers587778855
MSV3drs587778855
GWAS Ctlgrs587778855
Max Magnitude0
ClinVar
Risk rs587778855(T;T)
Alt rs587778855(T;T)
Reference rs587778855(A;A)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48941711A>T
CLNSRC
CLNACC RCV000114717.1,