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rs121913453

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913453(A;A)
Make rs121913453(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130862962
GeneABL1
is asnp
is mentioned by
dbSNPrs121913453
dbSNP (old)rs121913453
ClinGenrs121913453
ebirs121913453
HLIrs121913453
Exacrs121913453
Gnomadrs121913453
Varsomers121913453
Maprs121913453
PheGenIrs121913453
Biobankrs121913453
1000 genomesrs121913453
hgdprs121913453
ensemblrs121913453
gopubmedrs121913453
geneviewrs121913453
scholarrs121913453
googlers121913453
pharmgkbrs121913453
gwascentralrs121913453
openSNPrs121913453
23andMers121913453
23andMe allrs121913453
SNPshotrs121913453
SNPdbers121913453
MSV3drs121913453
GWAS Ctlgrs121913453
Max Magnitude0
ClinVar
Risk rs121913453(A;A)
Alt rs121913453(A;A)
Reference Rs121913453(G;G)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133738349G>A
CLNSRC
CLNACC RCV000430260.1,