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

rs587778838

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778838(A;A)
Make rs587778838(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48473359
GeneRB1
is asnp
is mentioned by
dbSNPrs587778838
ebirs587778838
HLIrs587778838
Exacrs587778838
Varsomers587778838
Maprs587778838
PheGenIrs587778838
hapmaprs587778838
1000 genomesrs587778838
hgdprs587778838
ensemblrs587778838
gopubmedrs587778838
geneviewrs587778838
scholarrs587778838
googlers587778838
pharmgkbrs587778838
gwascentralrs587778838
openSNPrs587778838
23andMers587778838
23andMe allrs587778838
SNP Nexus

SNPshotrs587778838
SNPdbers587778838
MSV3drs587778838
GWAS Ctlgrs587778838
Max Magnitude0
ClinVar
Risk rs587778838(A;A)
Alt rs587778838(A;A)
Reference rs587778838(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49047495G>A
CLNSRC
CLNACC RCV000114696.1,