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rs587778823

From SNPedia

Orientationplus
Geno Mag Summary
(CCG;CCG) 0 common in clinvar
Make rs587778823(-;-)
Make rs587778823(-;GCC)
Make rs587778823(GCC;GCC)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48303984
GeneLINC00441, RB1
is asnp
is mentioned by
dbSNPrs587778823
ebirs587778823
HLIrs587778823
Exacrs587778823
Varsomers587778823
Maprs587778823
PheGenIrs587778823
hapmaprs587778823
1000 genomesrs587778823
hgdprs587778823
ensemblrs587778823
gopubmedrs587778823
geneviewrs587778823
scholarrs587778823
googlers587778823
pharmgkbrs587778823
gwascentralrs587778823
openSNPrs587778823
23andMers587778823
23andMe allrs587778823
SNP Nexus

SNPshotrs587778823
SNPdbers587778823
MSV3drs587778823
GWAS Ctlgrs587778823
Max Magnitude0
ClinVar
Risk rs587778823(;)
Alt rs587778823(;)
Reference rs587778823(CCG;CCG)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene LINC00441 RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48878120_48878122delGCC
CLNSRC
CLNACC RCV000114709.1,