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rs137852729

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs137852729(-;-)
Make rs137852729(-;C)
Make rs137852729(C;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position33302346
GeneCEBPA, GPR84
is asnp
is mentioned by
dbSNPrs137852729
ebirs137852729
HLIrs137852729
Exacrs137852729
Varsomers137852729
Maprs137852729
PheGenIrs137852729
hapmaprs137852729
1000 genomesrs137852729
hgdprs137852729
ensemblrs137852729
gopubmedrs137852729
geneviewrs137852729
scholarrs137852729
googlers137852729
pharmgkbrs137852729
gwascentralrs137852729
openSNPrs137852729
23andMers137852729
23andMe allrs137852729
SNP Nexus

SNPshotrs137852729
SNPdbers137852729
MSV3drs137852729
GWAS Ctlgrs137852729
Max Magnitude0
ClinVar
Risk rs137852729(C;C)
Alt rs137852729(C;C)
Reference rs137852729(;)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene CEBPA CEBPA-AS1
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000019.9:g.33793253dupG
CLNSRC ClinVar GeneReviews
CLNACC RCV000020587.1,