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rs121913457

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913457(C;C)
Make rs121913457(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position130873004
GeneABL1
is asnp
is mentioned by
dbSNPrs121913457
ebirs121913457
HLIrs121913457
Exacrs121913457
Varsomers121913457
Maprs121913457
PheGenIrs121913457
hapmaprs121913457
1000 genomesrs121913457
hgdprs121913457
ensemblrs121913457
gopubmedrs121913457
geneviewrs121913457
scholarrs121913457
googlers121913457
pharmgkbrs121913457
gwascentralrs121913457
openSNPrs121913457
23andMers121913457
23andMe allrs121913457
SNP Nexus

SNPshotrs121913457
SNPdbers121913457
MSV3drs121913457
GWAS Ctlgrs121913457
Max Magnitude0
OMIM189980
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121913457(C;C)
Alt rs121913457(C;C)
Reference rs121913457(T;T)
Significance Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia, resistant to imatinib
Reversed 0
HGVS NC_000009.11:g.133748391T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013464.16,