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rs587778862

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587778862(-;-)
Make rs587778862(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48307361
GeneRB1
is asnp
is mentioned by
dbSNPrs587778862
dbSNP (old)rs587778862
ClinGenrs587778862
ebirs587778862
HLIrs587778862
Exacrs587778862
Gnomadrs587778862
Varsomers587778862
Maprs587778862
PheGenIrs587778862
Biobankrs587778862
1000 genomesrs587778862
hgdprs587778862
ensemblrs587778862
gopubmedrs587778862
geneviewrs587778862
scholarrs587778862
googlers587778862
pharmgkbrs587778862
gwascentralrs587778862
openSNPrs587778862
23andMers587778862
23andMe allrs587778862
SNP Nexus

SNPshotrs587778862
SNPdbers587778862
MSV3drs587778862
GWAS Ctlgrs587778862
Max Magnitude0
ClinVar
Risk rs587778862(-;-)
Alt rs587778862(-;-)
Reference Rs587778862(AG;AG)
Significance Pathogenic
Disease Retinoblastoma Hereditary cancer-predisposing syndrome
Variation info
Gene RB1
CLNDBN Retinoblastoma Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.48881497_48881498delAG
CLNSRC
CLNACC RCV000114738.1, RCV000492118.1,