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rs137853297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853297(A;A)
Make rs137853297(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position48456207
GeneRB1
is asnp
is mentioned by
dbSNPrs137853297
ebirs137853297
HLIrs137853297
Exacrs137853297
Varsomers137853297
Maprs137853297
PheGenIrs137853297
hapmaprs137853297
1000 genomesrs137853297
hgdprs137853297
ensemblrs137853297
gopubmedrs137853297
geneviewrs137853297
scholarrs137853297
googlers137853297
pharmgkbrs137853297
gwascentralrs137853297
openSNPrs137853297
23andMers137853297
23andMe allrs137853297
SNP Nexus

SNPshotrs137853297
SNPdbers137853297
MSV3drs137853297
GWAS Ctlgrs137853297
Max Magnitude0
OMIM180200
Desc
Variant0026
Relatedalso
ClinVar
Risk rs137853297(A;A)
Alt rs137853297(A;A)
Reference rs137853297(T;T)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49030343T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013970.2,