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rs587778867

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778867(A;T)
Make rs587778867(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48459686
GeneRB1
is asnp
is mentioned by
dbSNPrs587778867
ebirs587778867
HLIrs587778867
Exacrs587778867
Varsomers587778867
Maprs587778867
PheGenIrs587778867
hapmaprs587778867
1000 genomesrs587778867
hgdprs587778867
ensemblrs587778867
gopubmedrs587778867
geneviewrs587778867
scholarrs587778867
googlers587778867
pharmgkbrs587778867
gwascentralrs587778867
openSNPrs587778867
23andMers587778867
23andMe allrs587778867
SNP Nexus

SNPshotrs587778867
SNPdbers587778867
MSV3drs587778867
GWAS Ctlgrs587778867
Max Magnitude0
ClinVar
Risk rs587778867(T;T)
Alt rs587778867(T;T)
Reference rs587778867(A;A)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49033822A>T
CLNSRC
CLNACC RCV000114684.1,