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rs587778866

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778866(A;G)
Make rs587778866(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48456316
GeneRB1
is asnp
is mentioned by
dbSNPrs587778866
ebirs587778866
HLIrs587778866
Exacrs587778866
Varsomers587778866
Maprs587778866
PheGenIrs587778866
hapmaprs587778866
1000 genomesrs587778866
hgdprs587778866
ensemblrs587778866
gopubmedrs587778866
geneviewrs587778866
scholarrs587778866
googlers587778866
pharmgkbrs587778866
gwascentralrs587778866
openSNPrs587778866
23andMers587778866
23andMe allrs587778866
SNP Nexus

SNPshotrs587778866
SNPdbers587778866
MSV3drs587778866
GWAS Ctlgrs587778866
Max Magnitude0
ClinVar
Risk rs587778866(G;G)
Alt rs587778866(G;G)
Reference rs587778866(A;A)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49030452A>G
CLNSRC
CLNACC RCV000114682.1,