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rs121913460

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913460(A;T)
Make rs121913460(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130862971
GeneABL1
is asnp
is mentioned by
dbSNPrs121913460
dbSNP (old)rs121913460
ClinGenrs121913460
ebirs121913460
HLIrs121913460
Exacrs121913460
Gnomadrs121913460
Varsomers121913460
Maprs121913460
PheGenIrs121913460
Biobankrs121913460
1000 genomesrs121913460
hgdprs121913460
ensemblrs121913460
gopubmedrs121913460
geneviewrs121913460
scholarrs121913460
googlers121913460
pharmgkbrs121913460
gwascentralrs121913460
openSNPrs121913460
23andMers121913460
23andMe allrs121913460
SNPshotrs121913460
SNPdbers121913460
MSV3drs121913460
GWAS Ctlgrs121913460
Max Magnitude0
ClinVar
Risk rs121913460(T;T)
Alt rs121913460(T;T)
Reference Rs121913460(A;A)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133738358A>T
CLNSRC
CLNACC RCV000422595.1,