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rs587778859

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778859(A;A)
Make rs587778859(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48459828
GeneRB1
is asnp
is mentioned by
dbSNPrs587778859
ebirs587778859
HLIrs587778859
Exacrs587778859
Varsomers587778859
Maprs587778859
PheGenIrs587778859
hapmaprs587778859
1000 genomesrs587778859
hgdprs587778859
ensemblrs587778859
gopubmedrs587778859
geneviewrs587778859
scholarrs587778859
googlers587778859
pharmgkbrs587778859
gwascentralrs587778859
openSNPrs587778859
23andMers587778859
23andMe allrs587778859
SNP Nexus

SNPshotrs587778859
SNPdbers587778859
MSV3drs587778859
GWAS Ctlgrs587778859
Max Magnitude0
ClinVar
Risk rs587778859(A;A)
Alt rs587778859(A;A)
Reference rs587778859(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49033964G>A
CLNSRC
CLNACC RCV000114686.1,