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rs121913458

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913458(C;C)
Make rs121913458(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130862969
GeneABL1
is asnp
is mentioned by
dbSNPrs121913458
dbSNP (old)rs121913458
ClinGenrs121913458
ebirs121913458
HLIrs121913458
Exacrs121913458
Gnomadrs121913458
Varsomers121913458
Maprs121913458
PheGenIrs121913458
Biobankrs121913458
1000 genomesrs121913458
hgdprs121913458
ensemblrs121913458
gopubmedrs121913458
geneviewrs121913458
scholarrs121913458
googlers121913458
pharmgkbrs121913458
gwascentralrs121913458
openSNPrs121913458
23andMers121913458
23andMe allrs121913458
SNPshotrs121913458
SNPdbers121913458
MSV3drs121913458
GWAS Ctlgrs121913458
Max Magnitude0
ClinVar
Risk rs121913458(C;C) rs121913458(T;T)
Alt rs121913458(C;C) rs121913458(T;T)
Reference Rs121913458(G;G)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133738356G>C; NC_000009.11:g.133738356G>T
CLNSRC
CLNACC RCV000440949.1, RCV000422852.1,