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

rs587778869

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778869(C;T)
Make rs587778869(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48304015
GeneLINC00441, RB1
is asnp
is mentioned by
dbSNPrs587778869
ebirs587778869
HLIrs587778869
Exacrs587778869
Varsomers587778869
Maprs587778869
PheGenIrs587778869
hapmaprs587778869
1000 genomesrs587778869
hgdprs587778869
ensemblrs587778869
gopubmedrs587778869
geneviewrs587778869
scholarrs587778869
googlers587778869
pharmgkbrs587778869
gwascentralrs587778869
openSNPrs587778869
23andMers587778869
23andMe allrs587778869
SNP Nexus

SNPshotrs587778869
SNPdbers587778869
MSV3drs587778869
GWAS Ctlgrs587778869
Max Magnitude0
ClinVar
Risk rs587778869(T;T)
Alt rs587778869(T;T)
Reference rs587778869(C;C)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene LINC00441 RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48878151C>T
CLNSRC
CLNACC RCV000114710.1,