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rs587778871

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778871(A;A)
Make rs587778871(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48456354
GeneRB1
is asnp
is mentioned by
dbSNPrs587778871
ebirs587778871
HLIrs587778871
Exacrs587778871
Varsomers587778871
Maprs587778871
PheGenIrs587778871
hapmaprs587778871
1000 genomesrs587778871
hgdprs587778871
ensemblrs587778871
gopubmedrs587778871
geneviewrs587778871
scholarrs587778871
googlers587778871
pharmgkbrs587778871
gwascentralrs587778871
openSNPrs587778871
23andMers587778871
23andMe allrs587778871
SNP Nexus

SNPshotrs587778871
SNPdbers587778871
MSV3drs587778871
GWAS Ctlgrs587778871
Max Magnitude0
ClinVar
Risk rs587778871(A;A)
Alt rs587778871(A;A)
Reference rs587778871(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49030490G>A
CLNSRC
CLNACC RCV000114683.1,