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rs137853304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853304(C;C)
Make rs137853304(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position130872883
GeneABL1
is asnp
is mentioned by
dbSNPrs137853304
ebirs137853304
HLIrs137853304
Exacrs137853304
Varsomers137853304
Maprs137853304
PheGenIrs137853304
hapmaprs137853304
1000 genomesrs137853304
hgdprs137853304
ensemblrs137853304
gopubmedrs137853304
geneviewrs137853304
scholarrs137853304
googlers137853304
pharmgkbrs137853304
gwascentralrs137853304
openSNPrs137853304
23andMers137853304
23andMe allrs137853304
SNP Nexus

SNPshotrs137853304
SNPdbers137853304
MSV3drs137853304
GWAS Ctlgrs137853304
Max Magnitude0
OMIM189980
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853304(C;C)
Alt rs137853304(C;C)
Reference rs137853304(T;T)
Significance Pathogenic
Disease Chronic myeloid leukemia
Variation info
Gene ABL1
CLNDBN Chronic myeloid leukemia, resistant to imatinib
Reversed 0
HGVS NC_000009.11:g.133748270T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013463.23,