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rs121913448

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913448(A;A)
Make rs121913448(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position130862976
GeneABL1
is asnp
is mentioned by
dbSNPrs121913448
ebirs121913448
HLIrs121913448
Exacrs121913448
Varsomers121913448
Maprs121913448
PheGenIrs121913448
hapmaprs121913448
1000 genomesrs121913448
hgdprs121913448
ensemblrs121913448
gopubmedrs121913448
geneviewrs121913448
scholarrs121913448
googlers121913448
pharmgkbrs121913448
gwascentralrs121913448
openSNPrs121913448
23andMers121913448
23andMe allrs121913448
SNP Nexus

SNPshotrs121913448
SNPdbers121913448
MSV3drs121913448
GWAS Ctlgrs121913448
Max Magnitude0
OMIM189980
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913448(A;A)
Alt rs121913448(A;A)
Reference rs121913448(G;G)
Significance Pathogenic
Disease Leukemia
Variation info
Gene ABL1
CLNDBN Leukemia, philadelphia chromosome-positive, resistant to imatinib
Reversed 0
HGVS NC_000009.11:g.133738363G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013461.23,