Have questions? Visit https://www.reddit.com/r/SNPedia

rs587778870

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778870(C;G)
Make rs587778870(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48345145
GeneRB1
is asnp
is mentioned by
dbSNPrs587778870
ebirs587778870
HLIrs587778870
Exacrs587778870
Varsomers587778870
Maprs587778870
PheGenIrs587778870
hapmaprs587778870
1000 genomesrs587778870
hgdprs587778870
ensemblrs587778870
gopubmedrs587778870
geneviewrs587778870
scholarrs587778870
googlers587778870
pharmgkbrs587778870
gwascentralrs587778870
openSNPrs587778870
23andMers587778870
23andMe allrs587778870
SNP Nexus

SNPshotrs587778870
SNPdbers587778870
MSV3drs587778870
GWAS Ctlgrs587778870
Max Magnitude0
ClinVar
Risk rs587778870(G,T;G,T)
Alt rs587778870(G,T;G,T)
Reference rs587778870(C;C)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48919281C>G
CLNSRC
CLNACC RCV000114704.1,