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

rs121913450

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913450(A;G)
Make rs121913450(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130873016
GeneABL1
is asnp
is mentioned by
dbSNPrs121913450
dbSNP (classic)rs121913450
ClinGenrs121913450
ebirs121913450
HLIrs121913450
Exacrs121913450
Gnomadrs121913450
Varsomers121913450
LitVarrs121913450
Maprs121913450
PheGenIrs121913450
Biobankrs121913450
1000 genomesrs121913450
hgdprs121913450
ensemblrs121913450
geneviewrs121913450
scholarrs121913450
googlers121913450
pharmgkbrs121913450
gwascentralrs121913450
openSNPrs121913450
23andMers121913450
SNPshotrs121913450
SNPdbers121913450
MSV3drs121913450
GWAS Ctlgrs121913450
Max Magnitude0
ClinVar
Risk rs121913450(G;G)
Alt rs121913450(G;G)
Reference Rs121913450(A;A)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133748403A>G
CLNSRC
CLNACC RCV000427169.1,