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rs587778846

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778846(G;T)
Make rs587778846(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48377035
GeneRB1
is asnp
is mentioned by
dbSNPrs587778846
ebirs587778846
HLIrs587778846
Exacrs587778846
Varsomers587778846
Maprs587778846
PheGenIrs587778846
hapmaprs587778846
1000 genomesrs587778846
hgdprs587778846
ensemblrs587778846
gopubmedrs587778846
geneviewrs587778846
scholarrs587778846
googlers587778846
pharmgkbrs587778846
gwascentralrs587778846
openSNPrs587778846
23andMers587778846
23andMe allrs587778846
SNP Nexus

SNPshotrs587778846
SNPdbers587778846
MSV3drs587778846
GWAS Ctlgrs587778846
Max Magnitude0
ClinVar
Risk rs587778846(A,T;A,T)
Alt rs587778846(A,T;A,T)
Reference rs587778846(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48951171G>A; NC_000013.10:g.48951171G>T
CLNSRC
CLNACC RCV000114726.1, RCV000114727.1,