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

rs587778826

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778826(G;T)
Make rs587778826(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48347832
GeneRB1
is asnp
is mentioned by
dbSNPrs587778826
ebirs587778826
HLIrs587778826
Exacrs587778826
Varsomers587778826
Maprs587778826
PheGenIrs587778826
hapmaprs587778826
1000 genomesrs587778826
hgdprs587778826
ensemblrs587778826
gopubmedrs587778826
geneviewrs587778826
scholarrs587778826
googlers587778826
pharmgkbrs587778826
gwascentralrs587778826
openSNPrs587778826
23andMers587778826
23andMe allrs587778826
SNP Nexus

SNPshotrs587778826
SNPdbers587778826
MSV3drs587778826
GWAS Ctlgrs587778826
Max Magnitude0
ClinVar
Risk rs587778826(T;T)
Alt rs587778826(T;T)
Reference rs587778826(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48921968G>T
CLNSRC
CLNACC RCV000114706.1,