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rs137852732

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs137852732(-;-)
Make rs137852732(-;TG)
Make rs137852732(TG;TG)
ReferenceGRCh38 38.1/141
Chromosome19
Position33302095
GeneCEBPA, GPR84
is asnp
is mentioned by
dbSNPrs137852732
ebirs137852732
HLIrs137852732
Exacrs137852732
Varsomers137852732
Maprs137852732
PheGenIrs137852732
hapmaprs137852732
1000 genomesrs137852732
hgdprs137852732
ensemblrs137852732
gopubmedrs137852732
geneviewrs137852732
scholarrs137852732
googlers137852732
pharmgkbrs137852732
gwascentralrs137852732
openSNPrs137852732
23andMers137852732
23andMe allrs137852732
SNP Nexus

SNPshotrs137852732
SNPdbers137852732
MSV3drs137852732
GWAS Ctlgrs137852732
Max Magnitude0
ClinVar
Risk rs137852732(TG;TG)
Alt rs137852732(TG;TG)
Reference rs137852732(;)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene CEBPA CEBPA-AS1
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000019.9:g.33793002_33793003dupCA
CLNSRC ClinVar GeneReviews
CLNACC RCV000020585.1,