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rs387906517

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906517(A;A)
Make rs387906517(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position130862919
GeneABL1
is asnp
is mentioned by
dbSNPrs387906517
ClinGenrs387906517
ebirs387906517
HLIrs387906517
Exacrs387906517
Varsomers387906517
Maprs387906517
PheGenIrs387906517
hapmaprs387906517
1000 genomesrs387906517
hgdprs387906517
ensemblrs387906517
gopubmedrs387906517
geneviewrs387906517
scholarrs387906517
googlers387906517
pharmgkbrs387906517
gwascentralrs387906517
openSNPrs387906517
23andMers387906517
23andMe allrs387906517
SNP Nexus

SNPshotrs387906517
SNPdbers387906517
MSV3drs387906517
GWAS Ctlgrs387906517
Max Magnitude0
ClinVar
Risk rs387906517(A;A)
Alt rs387906517(A;A)
Reference Rs387906517(G;G)
Significance Pathogenic
Disease Leukemia
Variation info
Gene ABL1
CLNDBN Leukemia, Philadelphia chromosome-positive, resistant to imatinib
Reversed 0
HGVS NC_000009.11:g.133738306G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013461.24,