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rs587776784

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTTGAATCTG;CTTGAATCTG) 0 common in clinvar
Make rs587776784(-;-)
Make rs587776784(-;AATCTGCTTG)
Make rs587776784(AATCTGCTTG;AATCTGCTTG)
ReferenceGRCh38 38.1/142
Chromosome13
Position48453057
GeneRB1
is asnp
is mentioned by
dbSNPrs587776784
dbSNP (old)rs587776784
ClinGenrs587776784
ebirs587776784
HLIrs587776784
Exacrs587776784
Varsomers587776784
Maprs587776784
PheGenIrs587776784
Biobankrs587776784
1000 genomesrs587776784
hgdprs587776784
ensemblrs587776784
gopubmedrs587776784
geneviewrs587776784
scholarrs587776784
googlers587776784
pharmgkbrs587776784
gwascentralrs587776784
openSNPrs587776784
23andMers587776784
23andMe allrs587776784
SNP Nexus

SNPshotrs587776784
SNPdbers587776784
MSV3drs587776784
GWAS Ctlgrs587776784
Max Magnitude0
ClinVar
Risk rs587776784(-;-)
Alt rs587776784(-;-)
Reference Rs587776784(CTTGAATCTG;CTTGAATCTG)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49027193_49027202delAATCTGCTTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000013957.2,