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rs587776787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776787(A;A)
Make rs587776787(A;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position48463835
GeneRB1
is asnp
is mentioned by
dbSNPrs587776787
ebirs587776787
HLIrs587776787
Exacrs587776787
Varsomers587776787
Maprs587776787
PheGenIrs587776787
hapmaprs587776787
1000 genomesrs587776787
hgdprs587776787
ensemblrs587776787
gopubmedrs587776787
geneviewrs587776787
scholarrs587776787
googlers587776787
pharmgkbrs587776787
gwascentralrs587776787
openSNPrs587776787
23andMers587776787
23andMe allrs587776787
SNP Nexus

SNPshotrs587776787
SNPdbers587776787
MSV3drs587776787
GWAS Ctlgrs587776787
Max Magnitude0
ClinVar
Risk rs587776787(A;A)
Alt rs587776787(A;A)
Reference rs587776787(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49037971G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013964.2,