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rs587778834

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778834(A;A)
Make rs587778834(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48459700
GeneRB1
is asnp
is mentioned by
dbSNPrs587778834
ebirs587778834
HLIrs587778834
Exacrs587778834
Varsomers587778834
Maprs587778834
PheGenIrs587778834
hapmaprs587778834
1000 genomesrs587778834
hgdprs587778834
ensemblrs587778834
gopubmedrs587778834
geneviewrs587778834
scholarrs587778834
googlers587778834
pharmgkbrs587778834
gwascentralrs587778834
openSNPrs587778834
23andMers587778834
23andMe allrs587778834
SNP Nexus

SNPshotrs587778834
SNPdbers587778834
MSV3drs587778834
GWAS Ctlgrs587778834
Max Magnitude0
ClinVar
Risk rs587778834(A,T;A,T)
Alt rs587778834(A,T;A,T)
Reference rs587778834(C;C)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49033836C>A
CLNSRC
CLNACC RCV000114685.1,