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rs587778829

From SNPedia

Orientationplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs587778829(-;-)
Make rs587778829(-;CA)
Make rs587778829(CA;CA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48368537
GeneRB1
is asnp
is mentioned by
dbSNPrs587778829
ebirs587778829
HLIrs587778829
Exacrs587778829
Varsomers587778829
Maprs587778829
PheGenIrs587778829
hapmaprs587778829
1000 genomesrs587778829
hgdprs587778829
ensemblrs587778829
gopubmedrs587778829
geneviewrs587778829
scholarrs587778829
googlers587778829
pharmgkbrs587778829
gwascentralrs587778829
openSNPrs587778829
23andMers587778829
23andMe allrs587778829
SNP Nexus

SNPshotrs587778829
SNPdbers587778829
MSV3drs587778829
GWAS Ctlgrs587778829
Max Magnitude0
ClinVar
Risk rs587778829(;)
Alt rs587778829(;)
Reference rs587778829(AC;AC)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48942673_48942674delCA
CLNSRC
CLNACC RCV000114720.1,