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rs121913456

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913456(A;G)
Make rs121913456(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130862943
GeneABL1
is asnp
is mentioned by
dbSNPrs121913456
dbSNP (old)rs121913456
ClinGenrs121913456
ebirs121913456
HLIrs121913456
Exacrs121913456
Gnomadrs121913456
Varsomers121913456
Maprs121913456
PheGenIrs121913456
Biobankrs121913456
1000 genomesrs121913456
hgdprs121913456
ensemblrs121913456
gopubmedrs121913456
geneviewrs121913456
scholarrs121913456
googlers121913456
pharmgkbrs121913456
gwascentralrs121913456
openSNPrs121913456
23andMers121913456
23andMe allrs121913456
SNPshotrs121913456
SNPdbers121913456
MSV3drs121913456
GWAS Ctlgrs121913456
Max Magnitude0
ClinVar
Risk rs121913456(G;G)
Alt rs121913456(G;G)
Reference Rs121913456(A;A)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133738330A>G
CLNSRC
CLNACC RCV000440973.1,