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rs587778860

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778860(C;C)
Make rs587778860(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48463730
GeneRB1
is asnp
is mentioned by
dbSNPrs587778860
ebirs587778860
HLIrs587778860
Exacrs587778860
Varsomers587778860
Maprs587778860
PheGenIrs587778860
hapmaprs587778860
1000 genomesrs587778860
hgdprs587778860
ensemblrs587778860
gopubmedrs587778860
geneviewrs587778860
scholarrs587778860
googlers587778860
pharmgkbrs587778860
gwascentralrs587778860
openSNPrs587778860
23andMers587778860
23andMe allrs587778860
SNP Nexus

SNPshotrs587778860
SNPdbers587778860
MSV3drs587778860
GWAS Ctlgrs587778860
Max Magnitude0
ClinVar
Risk rs587778860(C;C)
Alt rs587778860(C;C)
Reference rs587778860(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49037866G>C
CLNSRC
CLNACC RCV000114687.1,