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rs587778832

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs587778832(-;-)
Make rs587778832(-;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48380199
GeneRB1
is asnp
is mentioned by
dbSNPrs587778832
ebirs587778832
HLIrs587778832
Exacrs587778832
Varsomers587778832
Maprs587778832
PheGenIrs587778832
hapmaprs587778832
1000 genomesrs587778832
hgdprs587778832
ensemblrs587778832
gopubmedrs587778832
geneviewrs587778832
scholarrs587778832
googlers587778832
pharmgkbrs587778832
gwascentralrs587778832
openSNPrs587778832
23andMers587778832
23andMe allrs587778832
SNP Nexus

SNPshotrs587778832
SNPdbers587778832
MSV3drs587778832
GWAS Ctlgrs587778832
Max Magnitude0
ClinVar
Risk rs587778832(;)
Alt rs587778832(;)
Reference rs587778832(TT;TT)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48954335_48954336delTT
CLNSRC
CLNACC RCV000114731.1,