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rs121913452

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913452(G;G)
Make rs121913452(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130873027
GeneABL1
is asnp
is mentioned by
dbSNPrs121913452
dbSNP (old)rs121913452
ClinGenrs121913452
ebirs121913452
HLIrs121913452
Exacrs121913452
Gnomadrs121913452
Varsomers121913452
Maprs121913452
PheGenIrs121913452
Biobankrs121913452
1000 genomesrs121913452
hgdprs121913452
ensemblrs121913452
gopubmedrs121913452
geneviewrs121913452
scholarrs121913452
googlers121913452
pharmgkbrs121913452
gwascentralrs121913452
openSNPrs121913452
23andMers121913452
23andMe allrs121913452
SNPshotrs121913452
SNPdbers121913452
MSV3drs121913452
GWAS Ctlgrs121913452
Max Magnitude0
ClinVar
Risk rs121913452(A;A) rs121913452(C;C) rs121913452(G;G)
Alt rs121913452(A;A) rs121913452(C;C) rs121913452(G;G)
Reference Rs121913452(T;T)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133748414T>A; NC_000009.11:g.133748414T>C; NC_000009.11:g.133748414T>G
CLNSRC
CLNACC RCV000424157.1, RCV000434412.1, RCV000437822.1,