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rs587778857

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778857(A;A)
Make rs587778857(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48381444
GeneRB1
is asnp
is mentioned by
dbSNPrs587778857
ebirs587778857
HLIrs587778857
Exacrs587778857
Varsomers587778857
Maprs587778857
PheGenIrs587778857
hapmaprs587778857
1000 genomesrs587778857
hgdprs587778857
ensemblrs587778857
gopubmedrs587778857
geneviewrs587778857
scholarrs587778857
googlers587778857
pharmgkbrs587778857
gwascentralrs587778857
openSNPrs587778857
23andMers587778857
23andMe allrs587778857
SNP Nexus

SNPshotrs587778857
SNPdbers587778857
MSV3drs587778857
GWAS Ctlgrs587778857
Max Magnitude0
ClinVar
Risk rs587778857(A;A)
Alt rs587778857(A;A)
Reference rs587778857(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48955580G>A
CLNSRC
CLNACC RCV000114736.1,