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rs587778840

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778840(-;-)
Make rs587778840(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48307359
GeneRB1
is asnp
is mentioned by
dbSNPrs587778840
ebirs587778840
HLIrs587778840
Exacrs587778840
Varsomers587778840
Maprs587778840
PheGenIrs587778840
hapmaprs587778840
1000 genomesrs587778840
hgdprs587778840
ensemblrs587778840
gopubmedrs587778840
geneviewrs587778840
scholarrs587778840
googlers587778840
pharmgkbrs587778840
gwascentralrs587778840
openSNPrs587778840
23andMers587778840
23andMe allrs587778840
SNP Nexus

SNPshotrs587778840
SNPdbers587778840
MSV3drs587778840
GWAS Ctlgrs587778840
Max Magnitude0
ClinVar
Risk rs587778840(;)
Alt rs587778840(;)
Reference rs587778840(A;A)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48881495delA
CLNSRC
CLNACC RCV000114737.1,