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rs587778831

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778831(A;A)
Make rs587778831(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48376917
GeneRB1
is asnp
is mentioned by
dbSNPrs587778831
ebirs587778831
HLIrs587778831
Exacrs587778831
Varsomers587778831
Maprs587778831
PheGenIrs587778831
hapmaprs587778831
1000 genomesrs587778831
hgdprs587778831
ensemblrs587778831
gopubmedrs587778831
geneviewrs587778831
scholarrs587778831
googlers587778831
pharmgkbrs587778831
gwascentralrs587778831
openSNPrs587778831
23andMers587778831
23andMe allrs587778831
SNP Nexus

SNPshotrs587778831
SNPdbers587778831
MSV3drs587778831
GWAS Ctlgrs587778831
Max Magnitude0
ClinVar
Risk rs587778831(A;A)
Alt rs587778831(A;A)
Reference rs587778831(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48951053G>A
CLNSRC
CLNACC RCV000114725.1,