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rs121913449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913449(A;T)
Make rs121913449(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position130862977
GeneABL1
is asnp
is mentioned by
dbSNPrs121913449
ebirs121913449
HLIrs121913449
Exacrs121913449
Varsomers121913449
Maprs121913449
PheGenIrs121913449
hapmaprs121913449
1000 genomesrs121913449
hgdprs121913449
ensemblrs121913449
gopubmedrs121913449
geneviewrs121913449
scholarrs121913449
googlers121913449
pharmgkbrs121913449
gwascentralrs121913449
openSNPrs121913449
23andMers121913449
23andMe allrs121913449
SNP Nexus

SNPshotrs121913449
SNPdbers121913449
MSV3drs121913449
GWAS Ctlgrs121913449
Max Magnitude0
OMIM189980
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121913449(T;T)
Alt rs121913449(T;T)
Reference rs121913449(A;A)
Significance Pathogenic
Disease Leukemia
Variation info
Gene ABL1
CLNDBN Leukemia, philadelphia chromosome-positive, resistant to imatinib
Reversed 0
HGVS NC_000009.11:g.133738364A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013460.21,