Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519758

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519758(G;G)
Make rs1057519758(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130872153
GeneABL1
is asnp
is mentioned by
dbSNPrs1057519758
dbSNP (classic)rs1057519758
ClinGenrs1057519758
ebirs1057519758
HLIrs1057519758
Exacrs1057519758
Gnomadrs1057519758
Varsomers1057519758
LitVarrs1057519758
Maprs1057519758
PheGenIrs1057519758
Biobankrs1057519758
1000 genomesrs1057519758
hgdprs1057519758
ensemblrs1057519758
geneviewrs1057519758
scholarrs1057519758
googlers1057519758
pharmgkbrs1057519758
gwascentralrs1057519758
openSNPrs1057519758
23andMers1057519758
SNPshotrs1057519758
SNPdbers1057519758
MSV3drs1057519758
GWAS Ctlgrs1057519758
Max Magnitude0
ClinVar
Risk rs1057519758(G;G)
Alt rs1057519758(G;G)
Reference Rs1057519758(T;T)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133747540T>G
CLNSRC
CLNACC RCV000424931.1,