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rs121913454

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913454(A;G)
Make rs121913454(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130874969
GeneABL1
is asnp
is mentioned by
dbSNPrs121913454
dbSNP (old)rs121913454
ClinGenrs121913454
ebirs121913454
HLIrs121913454
Exacrs121913454
Gnomadrs121913454
Varsomers121913454
LitVarrs121913454
Maprs121913454
PheGenIrs121913454
Biobankrs121913454
1000 genomesrs121913454
hgdprs121913454
ensemblrs121913454
gopubmedrs121913454
geneviewrs121913454
scholarrs121913454
googlers121913454
pharmgkbrs121913454
gwascentralrs121913454
openSNPrs121913454
23andMers121913454
23andMe allrs121913454
SNPshotrs121913454
SNPdbers121913454
MSV3drs121913454
GWAS Ctlgrs121913454
Max Magnitude0
ClinVar
Risk rs121913454(G;G)
Alt rs121913454(G;G)
Reference Rs121913454(A;A)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133750356A>G
CLNSRC
CLNACC RCV000419848.1,