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rs387906516

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906516(A;T)
Make rs387906516(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position130862920
GeneABL1
is asnp
is mentioned by
dbSNPrs387906516
ebirs387906516
HLIrs387906516
Exacrs387906516
Varsomers387906516
Maprs387906516
PheGenIrs387906516
hapmaprs387906516
1000 genomesrs387906516
hgdprs387906516
ensemblrs387906516
gopubmedrs387906516
geneviewrs387906516
scholarrs387906516
googlers387906516
pharmgkbrs387906516
gwascentralrs387906516
openSNPrs387906516
23andMers387906516
23andMe allrs387906516
SNP Nexus

SNPshotrs387906516
SNPdbers387906516
MSV3drs387906516
GWAS Ctlgrs387906516
Max Magnitude0
ClinVar
Risk rs387906516(T;T)
Alt rs387906516(T;T)
Reference rs387906516(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.133738307A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013460.22,