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

rs587778824

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778824(-;-)
Make rs587778824(-;TA)
Make rs587778824(TA;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48307370
GeneRB1
is asnp
is mentioned by
dbSNPrs587778824
ebirs587778824
HLIrs587778824
Exacrs587778824
Varsomers587778824
Maprs587778824
PheGenIrs587778824
hapmaprs587778824
1000 genomesrs587778824
hgdprs587778824
ensemblrs587778824
gopubmedrs587778824
geneviewrs587778824
scholarrs587778824
googlers587778824
pharmgkbrs587778824
gwascentralrs587778824
openSNPrs587778824
23andMers587778824
23andMe allrs587778824
SNP Nexus

SNPshotrs587778824
SNPdbers587778824
MSV3drs587778824
GWAS Ctlgrs587778824
Max Magnitude0
ClinVar
Risk rs587778824(TA;TA)
Alt rs587778824(TA;TA)
Reference rs587778824(;)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48881505_48881506dupTA
CLNSRC
CLNACC RCV000114739.1,