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rs587778863

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778863(A;A)
Make rs587778863(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48381436
GeneRB1
is asnp
is mentioned by
dbSNPrs587778863
ebirs587778863
HLIrs587778863
Exacrs587778863
Varsomers587778863
Maprs587778863
PheGenIrs587778863
hapmaprs587778863
1000 genomesrs587778863
hgdprs587778863
ensemblrs587778863
gopubmedrs587778863
geneviewrs587778863
scholarrs587778863
googlers587778863
pharmgkbrs587778863
gwascentralrs587778863
openSNPrs587778863
23andMers587778863
23andMe allrs587778863
SNP Nexus

SNPshotrs587778863
SNPdbers587778863
MSV3drs587778863
GWAS Ctlgrs587778863
Max Magnitude0
ClinVar
Risk rs587778863(A;A)
Alt rs587778863(A;A)
Reference rs587778863(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48955572G>A
CLNSRC
CLNACC RCV000114735.1,