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rs1057519773

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519773(A;A)
Make rs1057519773(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130872901
GeneABL1
is asnp
is mentioned by
dbSNPrs1057519773
dbSNP (old)rs1057519773
ClinGenrs1057519773
ebirs1057519773
HLIrs1057519773
Exacrs1057519773
Gnomadrs1057519773
Varsomers1057519773
Maprs1057519773
PheGenIrs1057519773
Biobankrs1057519773
1000 genomesrs1057519773
hgdprs1057519773
ensemblrs1057519773
gopubmedrs1057519773
geneviewrs1057519773
scholarrs1057519773
googlers1057519773
pharmgkbrs1057519773
gwascentralrs1057519773
openSNPrs1057519773
23andMers1057519773
23andMe allrs1057519773
SNPshotrs1057519773
SNPdbers1057519773
MSV3drs1057519773
GWAS Ctlgrs1057519773
Max Magnitude0
ClinVar
Risk rs1057519773(A;A) rs1057519773(C;C) rs1057519773(G;G)
Alt rs1057519773(A;A) rs1057519773(C;C) rs1057519773(G;G)
Reference Rs1057519773(T;T)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133748288T>A; NC_000009.11:g.133748288T>C; NC_000009.11:g.133748288T>G
CLNSRC
CLNACC RCV000421381.1, RCV000444847.1, RCV000430721.1,