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rs587778827

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778827(-;-)
Make rs587778827(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48362891
GeneRB1
is asnp
is mentioned by
dbSNPrs587778827
ebirs587778827
HLIrs587778827
Exacrs587778827
Varsomers587778827
Maprs587778827
PheGenIrs587778827
hapmaprs587778827
1000 genomesrs587778827
hgdprs587778827
ensemblrs587778827
gopubmedrs587778827
geneviewrs587778827
scholarrs587778827
googlers587778827
pharmgkbrs587778827
gwascentralrs587778827
openSNPrs587778827
23andMers587778827
23andMe allrs587778827
SNP Nexus

SNPshotrs587778827
SNPdbers587778827
MSV3drs587778827
GWAS Ctlgrs587778827
Max Magnitude0
ClinVar
Risk rs587778827(;)
Alt rs587778827(;)
Reference rs587778827(A;A)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48937027delA
CLNSRC
CLNACC RCV000114713.1,