Have questions? Visit https://www.reddit.com/r/SNPedia

rs137853294

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853294(C;T)
Make rs137853294(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position48459708
GeneRB1
is asnp
is mentioned by
dbSNPrs137853294
ebirs137853294
HLIrs137853294
Exacrs137853294
Varsomers137853294
Maprs137853294
PheGenIrs137853294
hapmaprs137853294
1000 genomesrs137853294
hgdprs137853294
ensemblrs137853294
gopubmedrs137853294
geneviewrs137853294
scholarrs137853294
googlers137853294
pharmgkbrs137853294
gwascentralrs137853294
openSNPrs137853294
23andMers137853294
23andMe allrs137853294
SNP Nexus

SNPshotrs137853294
SNPdbers137853294
MSV3drs137853294
GWAS Ctlgrs137853294
Max Magnitude0
OMIM180200
Desc
Variant0019
Relatedalso
ClinVar
Risk rs137853294(T;T)
Alt rs137853294(T;T)
Reference rs137853294(C;C)
Significance Pathogenic
Disease Retinoblastoma not provided
Variation info
Gene RB1
CLNDBN Retinoblastoma not provided
Reversed 0
HGVS NC_000013.10:g.49033844C>T
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000013962.3, RCV000078635.3,