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rs587778828

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778828(-;-)
Make rs587778828(-;A)
Make rs587778828(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48364916
GeneRB1
is asnp
is mentioned by
dbSNPrs587778828
ebirs587778828
HLIrs587778828
Exacrs587778828
Varsomers587778828
Maprs587778828
PheGenIrs587778828
hapmaprs587778828
1000 genomesrs587778828
hgdprs587778828
ensemblrs587778828
gopubmedrs587778828
geneviewrs587778828
scholarrs587778828
googlers587778828
pharmgkbrs587778828
gwascentralrs587778828
openSNPrs587778828
23andMers587778828
23andMe allrs587778828
SNP Nexus

SNPshotrs587778828
SNPdbers587778828
MSV3drs587778828
GWAS Ctlgrs587778828
Max Magnitude0
ClinVar
Risk rs587778828(A;A)
Alt rs587778828(A;A)
Reference rs587778828(;)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48939052dupA
CLNSRC
CLNACC RCV000114714.1,