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rs587778837

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778837(-;-)
Make rs587778837(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48465332
GeneRB1
is asnp
is mentioned by
dbSNPrs587778837
ebirs587778837
HLIrs587778837
Exacrs587778837
Varsomers587778837
Maprs587778837
PheGenIrs587778837
hapmaprs587778837
1000 genomesrs587778837
hgdprs587778837
ensemblrs587778837
gopubmedrs587778837
geneviewrs587778837
scholarrs587778837
googlers587778837
pharmgkbrs587778837
gwascentralrs587778837
openSNPrs587778837
23andMers587778837
23andMe allrs587778837
SNP Nexus

SNPshotrs587778837
SNPdbers587778837
MSV3drs587778837
GWAS Ctlgrs587778837
Max Magnitude0
ClinVar
Risk rs587778837(;)
Alt rs587778837(;)
Reference rs587778837(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49039468delG
CLNSRC
CLNACC RCV000114695.1,