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rs121913297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913297(G;T)
Make rs121913297(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position48465028
GeneRB1
is asnp
is mentioned by
dbSNPrs121913297
ebirs121913297
HLIrs121913297
Exacrs121913297
Varsomers121913297
Maprs121913297
PheGenIrs121913297
hapmaprs121913297
1000 genomesrs121913297
hgdprs121913297
ensemblrs121913297
gopubmedrs121913297
geneviewrs121913297
scholarrs121913297
googlers121913297
pharmgkbrs121913297
gwascentralrs121913297
openSNPrs121913297
23andMers121913297
23andMe allrs121913297
SNP Nexus

SNPshotrs121913297
SNPdbers121913297
MSV3drs121913297
GWAS Ctlgrs121913297
Max Magnitude0
OMIM180200
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121913297(T;T)
Alt rs121913297(T;T)
Reference rs121913297(G;G)
Significance Pathogenic
Disease Small cell lung cancer
Variation info
Gene RB1
CLNDBN Small cell lung cancer
Reversed 0
HGVS NC_000013.10:g.49039164G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013953.4,