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rs587778845

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778845(A;A)
Make rs587778845(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48373443
GeneRB1
is asnp
is mentioned by
dbSNPrs587778845
ebirs587778845
HLIrs587778845
Exacrs587778845
Varsomers587778845
Maprs587778845
PheGenIrs587778845
hapmaprs587778845
1000 genomesrs587778845
hgdprs587778845
ensemblrs587778845
gopubmedrs587778845
geneviewrs587778845
scholarrs587778845
googlers587778845
pharmgkbrs587778845
gwascentralrs587778845
openSNPrs587778845
23andMers587778845
23andMe allrs587778845
SNP Nexus

SNPshotrs587778845
SNPdbers587778845
MSV3drs587778845
GWAS Ctlgrs587778845
Max Magnitude0
ClinVar
Risk rs587778845(A;A)
Alt rs587778845(A;A)
Reference rs587778845(T;T)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48947579T>A
CLNSRC
CLNACC RCV000114723.1,