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rs121913451

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913451(C;G)
Make rs121913451(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130872903
GeneABL1
is asnp
is mentioned by
dbSNPrs121913451
dbSNP (old)rs121913451
ClinGenrs121913451
ebirs121913451
HLIrs121913451
Exacrs121913451
Gnomadrs121913451
Varsomers121913451
Maprs121913451
PheGenIrs121913451
Biobankrs121913451
1000 genomesrs121913451
hgdprs121913451
ensemblrs121913451
gopubmedrs121913451
geneviewrs121913451
scholarrs121913451
googlers121913451
pharmgkbrs121913451
gwascentralrs121913451
openSNPrs121913451
23andMers121913451
23andMe allrs121913451
SNPshotrs121913451
SNPdbers121913451
MSV3drs121913451
GWAS Ctlgrs121913451
Max Magnitude0
ClinVar
Risk rs121913451(A;A) rs121913451(G;G)
Alt rs121913451(A;A) rs121913451(G;G)
Reference Rs121913451(C;C)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133748290C>A; NC_000009.11:g.133748290C>G
CLNSRC
CLNACC RCV000424701.1, RCV000438035.1,