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

rs121913455

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913455(C;G)
Make rs121913455(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position130862955
GeneABL1
is asnp
is mentioned by
dbSNPrs121913455
dbSNP (classic)rs121913455
ClinGenrs121913455
ebirs121913455
HLIrs121913455
Exacrs121913455
Gnomadrs121913455
Varsomers121913455
LitVarrs121913455
Maprs121913455
PheGenIrs121913455
Biobankrs121913455
1000 genomesrs121913455
hgdprs121913455
ensemblrs121913455
geneviewrs121913455
scholarrs121913455
googlers121913455
pharmgkbrs121913455
gwascentralrs121913455
openSNPrs121913455
23andMers121913455
23andMe allrs121913455
SNPshotrs121913455
SNPdbers121913455
MSV3drs121913455
GWAS Ctlgrs121913455
Max Magnitude0
ClinVar
Risk rs121913455(G;G)
Alt rs121913455(G;G)
Reference Rs121913455(C;C)
Significance Probable-Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia
Reversed 0
HGVS NC_000009.11:g.133738342C>G
CLNSRC
CLNACC RCV000420247.1,