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rs137852733

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs137852733(-;-)
Make rs137852733(-;C)
Make rs137852733(C;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position33302197
GeneCEBPA
is asnp
is mentioned by
dbSNPrs137852733
ebirs137852733
HLIrs137852733
Exacrs137852733
Varsomers137852733
Maprs137852733
PheGenIrs137852733
hapmaprs137852733
1000 genomesrs137852733
hgdprs137852733
ensemblrs137852733
gopubmedrs137852733
geneviewrs137852733
scholarrs137852733
googlers137852733
pharmgkbrs137852733
gwascentralrs137852733
openSNPrs137852733
23andMers137852733
23andMe allrs137852733
SNP Nexus

SNPshotrs137852733
SNPdbers137852733
MSV3drs137852733
GWAS Ctlgrs137852733
Max Magnitude0
ClinVar
Risk rs137852733(C;C)
Alt rs137852733(C;C)
Reference rs137852733(;)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene CEBPA CEBPA-AS1
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000019.9:g.33793103_33793104insG
CLNSRC ClinVar GeneReviews
CLNACC RCV000020584.1,


OMIM601626
Desc
Variant
Relatedalso