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rs137852728

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852728(-;-)
Make rs137852728(-;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position33302347
GeneCEBPA
is asnp
is mentioned by
dbSNPrs137852728
ebirs137852728
HLIrs137852728
Exacrs137852728
Varsomers137852728
Maprs137852728
PheGenIrs137852728
hapmaprs137852728
1000 genomesrs137852728
hgdprs137852728
ensemblrs137852728
gopubmedrs137852728
geneviewrs137852728
scholarrs137852728
googlers137852728
pharmgkbrs137852728
gwascentralrs137852728
openSNPrs137852728
23andMers137852728
23andMe allrs137852728
SNP Nexus

SNPshotrs137852728
SNPdbers137852728
MSV3drs137852728
GWAS Ctlgrs137852728
Max Magnitude0
ClinVar
Risk rs137852728(;)
Alt rs137852728(;)
Reference rs137852728(C;C)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene CEBPA CEBPA-AS1
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000019.9:g.33793253delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000019132.33,


OMIM601626
Desc
Variant
Relatedalso