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rs121913459

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913459(C;T)
Make rs121913459(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position130872896
GeneABL1
is asnp
is mentioned by
dbSNPrs121913459
ebirs121913459
HLIrs121913459
Exacrs121913459
Varsomers121913459
Maprs121913459
PheGenIrs121913459
hapmaprs121913459
1000 genomesrs121913459
hgdprs121913459
ensemblrs121913459
gopubmedrs121913459
geneviewrs121913459
scholarrs121913459
googlers121913459
pharmgkbrs121913459
gwascentralrs121913459
openSNPrs121913459
23andMers121913459
23andMe allrs121913459
SNP Nexus

SNPshotrs121913459
SNPdbers121913459
MSV3drs121913459
GWAS Ctlgrs121913459
Max Magnitude0
OMIM189980
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121913459(T;T)
Alt rs121913459(T;T)
Reference rs121913459(C;C)
Significance Pathogenic
Disease Leukemia
Variation info
Gene ABL1
CLNDBN Leukemia, Philadelphia chromosome-positive, resistant to imatinib
Reversed 0
HGVS NC_000009.11:g.133748283C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013459.24,