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rs1057519772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519772(A;G)
Make rs1057519772(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130872895
GeneABL1
is asnp
is mentioned by
dbSNPrs1057519772
dbSNP (classic)rs1057519772
ClinGenrs1057519772
ebirs1057519772
HLIrs1057519772
Exacrs1057519772
Gnomadrs1057519772
Varsomers1057519772
LitVarrs1057519772
Maprs1057519772
PheGenIrs1057519772
Biobankrs1057519772
1000 genomesrs1057519772
hgdprs1057519772
ensemblrs1057519772
geneviewrs1057519772
scholarrs1057519772
googlers1057519772
pharmgkbrs1057519772
gwascentralrs1057519772
openSNPrs1057519772
23andMers1057519772
SNPshotrs1057519772
SNPdbers1057519772
MSV3drs1057519772
GWAS Ctlgrs1057519772
Max Magnitude0
ClinVar
Risk rs1057519772(G;G)
Alt rs1057519772(G;G)
Reference Rs1057519772(A;A)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133748282A>G
CLNSRC
CLNACC RCV000438506.1,