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

rs587778830

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778830(-;-)
Make rs587778830(-;C)
Make rs587778830(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48373424
GeneRB1
is asnp
is mentioned by
dbSNPrs587778830
ebirs587778830
HLIrs587778830
Exacrs587778830
Varsomers587778830
Maprs587778830
PheGenIrs587778830
hapmaprs587778830
1000 genomesrs587778830
hgdprs587778830
ensemblrs587778830
gopubmedrs587778830
geneviewrs587778830
scholarrs587778830
googlers587778830
pharmgkbrs587778830
gwascentralrs587778830
openSNPrs587778830
23andMers587778830
23andMe allrs587778830
SNP Nexus

SNPshotrs587778830
SNPdbers587778830
MSV3drs587778830
GWAS Ctlgrs587778830
Max Magnitude0
ClinVar
Risk rs587778830(C;C)
Alt rs587778830(C;C)
Reference rs587778830(;)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48947560dupC
CLNSRC
CLNACC RCV000114722.1,