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rs587778849

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778849(A;T)
Make rs587778849(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48463788
GeneRB1
is asnp
is mentioned by
dbSNPrs587778849
ebirs587778849
HLIrs587778849
Exacrs587778849
Varsomers587778849
Maprs587778849
PheGenIrs587778849
hapmaprs587778849
1000 genomesrs587778849
hgdprs587778849
ensemblrs587778849
gopubmedrs587778849
geneviewrs587778849
scholarrs587778849
googlers587778849
pharmgkbrs587778849
gwascentralrs587778849
openSNPrs587778849
23andMers587778849
23andMe allrs587778849
SNP Nexus

SNPshotrs587778849
SNPdbers587778849
MSV3drs587778849
GWAS Ctlgrs587778849
Max Magnitude0
ClinVar
Risk rs587778849(T;T)
Alt rs587778849(T;T)
Reference rs587778849(A;A)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49037924A>T
CLNSRC
CLNACC RCV000114688.1,