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rs587778843

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778843(G;T)
Make rs587778843(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48364969
GeneRB1
is asnp
is mentioned by
dbSNPrs587778843
ebirs587778843
HLIrs587778843
Exacrs587778843
Varsomers587778843
Maprs587778843
PheGenIrs587778843
hapmaprs587778843
1000 genomesrs587778843
hgdprs587778843
ensemblrs587778843
gopubmedrs587778843
geneviewrs587778843
scholarrs587778843
googlers587778843
pharmgkbrs587778843
gwascentralrs587778843
openSNPrs587778843
23andMers587778843
23andMe allrs587778843
SNP Nexus

SNPshotrs587778843
SNPdbers587778843
MSV3drs587778843
GWAS Ctlgrs587778843
Max Magnitude0
ClinVar
Risk rs587778843(T;T)
Alt rs587778843(T;T)
Reference rs587778843(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48939105G>T
CLNSRC
CLNACC RCV000114715.1,