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rs587776785

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTTATAAAA;TTTATAAAA) 0 common in clinvar
Make rs587776785(-;-)
Make rs587776785(-;TTTATAAAA)
ReferenceGRCh38 38.1/142
Chromosome13
Position48456338
GeneRB1
is asnp
is mentioned by
dbSNPrs587776785
ebirs587776785
HLIrs587776785
Exacrs587776785
Varsomers587776785
Maprs587776785
PheGenIrs587776785
hapmaprs587776785
1000 genomesrs587776785
hgdprs587776785
ensemblrs587776785
gopubmedrs587776785
geneviewrs587776785
scholarrs587776785
googlers587776785
pharmgkbrs587776785
gwascentralrs587776785
openSNPrs587776785
23andMers587776785
23andMe allrs587776785
SNP Nexus

SNPshotrs587776785
SNPdbers587776785
MSV3drs587776785
GWAS Ctlgrs587776785
Max Magnitude0
ClinVar
Risk rs587776785(;)
Alt rs587776785(;)
Reference rs587776785(TTTATAAAA;TTTATAAAA)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49030474_49030482delTTTATAAAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000013958.2,