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rs587778861

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778861(A;A)
Make rs587778861(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48465033
GeneRB1
is asnp
is mentioned by
dbSNPrs587778861
ebirs587778861
HLIrs587778861
Exacrs587778861
Varsomers587778861
Maprs587778861
PheGenIrs587778861
hapmaprs587778861
1000 genomesrs587778861
hgdprs587778861
ensemblrs587778861
gopubmedrs587778861
geneviewrs587778861
scholarrs587778861
googlers587778861
pharmgkbrs587778861
gwascentralrs587778861
openSNPrs587778861
23andMers587778861
23andMe allrs587778861
SNP Nexus

SNPshotrs587778861
SNPdbers587778861
MSV3drs587778861
GWAS Ctlgrs587778861
Max Magnitude0
ClinVar
Risk rs587778861(A,C;A,C)
Alt rs587778861(A,C;A,C)
Reference rs587778861(T;T)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49039169T>A
CLNSRC
CLNACC RCV000114693.1,