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rs587778836

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778836(-;-)
Make rs587778836(-;TTGA)
Make rs587778836(TTGA;TTGA)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48465016
GeneRB1
is asnp
is mentioned by
dbSNPrs587778836
ebirs587778836
HLIrs587778836
Exacrs587778836
Varsomers587778836
Maprs587778836
PheGenIrs587778836
hapmaprs587778836
1000 genomesrs587778836
hgdprs587778836
ensemblrs587778836
gopubmedrs587778836
geneviewrs587778836
scholarrs587778836
googlers587778836
pharmgkbrs587778836
gwascentralrs587778836
openSNPrs587778836
23andMers587778836
23andMe allrs587778836
SNP Nexus

SNPshotrs587778836
SNPdbers587778836
MSV3drs587778836
GWAS Ctlgrs587778836
Max Magnitude0
ClinVar
Risk rs587778836(TTGA;TTGA)
Alt rs587778836(TTGA;TTGA)
Reference rs587778836(;)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49039149_49039152dupTTGA
CLNSRC
CLNACC RCV000114692.1,