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rs137852730

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852730(-;-)
Make rs137852730(-;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position33302274
GeneCEBPA
is asnp
is mentioned by
dbSNPrs137852730
ebirs137852730
HLIrs137852730
Exacrs137852730
Varsomers137852730
Maprs137852730
PheGenIrs137852730
hapmaprs137852730
1000 genomesrs137852730
hgdprs137852730
ensemblrs137852730
gopubmedrs137852730
geneviewrs137852730
scholarrs137852730
googlers137852730
pharmgkbrs137852730
gwascentralrs137852730
openSNPrs137852730
23andMers137852730
23andMe allrs137852730
SNP Nexus

SNPshotrs137852730
SNPdbers137852730
MSV3drs137852730
GWAS Ctlgrs137852730
Max Magnitude0
ClinVar
Risk rs137852730(;)
Alt rs137852730(;)
Reference rs137852730(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.33793180delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000020582.1,


OMIM601626
Desc
Variant
Relatedalso