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rs1057519775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519775(G;G)
Make rs1057519775(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130873028
GeneABL1
is asnp
is mentioned by
dbSNPrs1057519775
dbSNP (classic)rs1057519775
ClinGenrs1057519775
ebirs1057519775
HLIrs1057519775
Exacrs1057519775
Gnomadrs1057519775
Varsomers1057519775
LitVarrs1057519775
Maprs1057519775
PheGenIrs1057519775
Biobankrs1057519775
1000 genomesrs1057519775
hgdprs1057519775
ensemblrs1057519775
geneviewrs1057519775
scholarrs1057519775
googlers1057519775
pharmgkbrs1057519775
gwascentralrs1057519775
openSNPrs1057519775
23andMers1057519775
SNPshotrs1057519775
SNPdbers1057519775
MSV3drs1057519775
GWAS Ctlgrs1057519775
Max Magnitude0
ClinVar
Risk rs1057519775(G;G)
Alt rs1057519775(G;G)
Reference Rs1057519775(T;T)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133748415T>G
CLNSRC
CLNACC RCV000442919.1,