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rs121913461

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913461(C;C)
Make rs121913461(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position130862970
GeneABL1
is asnp
is mentioned by
dbSNPrs121913461
ebirs121913461
HLIrs121913461
Exacrs121913461
Varsomers121913461
Maprs121913461
PheGenIrs121913461
hapmaprs121913461
1000 genomesrs121913461
hgdprs121913461
ensemblrs121913461
gopubmedrs121913461
geneviewrs121913461
scholarrs121913461
googlers121913461
pharmgkbrs121913461
gwascentralrs121913461
openSNPrs121913461
23andMers121913461
23andMe allrs121913461
SNP Nexus

SNPshotrs121913461
SNPdbers121913461
MSV3drs121913461
GWAS Ctlgrs121913461
Max Magnitude0
OMIM189980
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121913461(C;C)
Alt rs121913461(C;C)
Reference rs121913461(T;T)
Significance Pathogenic
Disease Leukemia
Variation info
Gene ABL1
CLNDBN Leukemia, Philadelphia chromosome-positive, resistant to imatinib
Reversed 0
HGVS NC_000009.11:g.133738357T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013462.24,