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rs398123332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123332(-;-)
Make rs398123332(-;T)
Make rs398123332(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position48381333
GeneRB1
is asnp
is mentioned by
dbSNPrs398123332
ebirs398123332
HLIrs398123332
Exacrs398123332
Varsomers398123332
Maprs398123332
PheGenIrs398123332
hapmaprs398123332
1000 genomesrs398123332
hgdprs398123332
ensemblrs398123332
gopubmedrs398123332
geneviewrs398123332
scholarrs398123332
googlers398123332
pharmgkbrs398123332
gwascentralrs398123332
openSNPrs398123332
23andMers398123332
23andMe allrs398123332
SNP Nexus

SNPshotrs398123332
SNPdbers398123332
MSV3drs398123332
GWAS Ctlgrs398123332
Max Magnitude0
ClinVar
Risk rs398123332(T;T)
Alt rs398123332(T;T)
Reference rs398123332(;)
Significance Pathogenic
Disease not provided Retinoblastoma
Variation info
Gene RB1
CLNDBN not provided Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48955469dupT
CLNSRC HGMD
CLNACC RCV000078634.3, RCV000175134.1,