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rs137853295

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853295(G;T)
Make rs137853295(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position48459750
GeneRB1
is asnp
is mentioned by
dbSNPrs137853295
ebirs137853295
HLIrs137853295
Exacrs137853295
Varsomers137853295
Maprs137853295
PheGenIrs137853295
hapmaprs137853295
1000 genomesrs137853295
hgdprs137853295
ensemblrs137853295
gopubmedrs137853295
geneviewrs137853295
scholarrs137853295
googlers137853295
pharmgkbrs137853295
gwascentralrs137853295
openSNPrs137853295
23andMers137853295
23andMe allrs137853295
SNP Nexus

SNPshotrs137853295
SNPdbers137853295
MSV3drs137853295
GWAS Ctlgrs137853295
Max Magnitude0
OMIM180200
Desc
Variant0020
Relatedalso
ClinVar
Risk rs137853295(T;T)
Alt rs137853295(T;T)
Reference rs137853295(G;G)
Significance Untested
Disease
Variation info
Gene RB1
CLNDBN
Reversed 0
HGVS NC_000013.10:g.49033886G>T
CLNSRC
CLNACC