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rs587776849

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776849(-;-)
Make rs587776849(-;CGGC)
Make rs587776849(CGGC;CGGC)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position33302204
GeneCEBPA, CEBPA-AS1
is asnp
is mentioned by
dbSNPrs587776849
ebirs587776849
HLIrs587776849
Exacrs587776849
Varsomers587776849
Maprs587776849
PheGenIrs587776849
hapmaprs587776849
1000 genomesrs587776849
hgdprs587776849
ensemblrs587776849
gopubmedrs587776849
geneviewrs587776849
scholarrs587776849
googlers587776849
pharmgkbrs587776849
gwascentralrs587776849
openSNPrs587776849
23andMers587776849
23andMe allrs587776849
SNP Nexus

SNPshotrs587776849
SNPdbers587776849
MSV3drs587776849
GWAS Ctlgrs587776849
Max Magnitude0
ClinVar
Risk rs587776849(CGGC;CGGC)
Alt rs587776849(CGGC;CGGC)
Reference rs587776849(;)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene CEBPA CEBPA-AS1
CLNDBN Acute myeloid leukemia
Reversed 0
HGVS NC_000019.9:g.33793107_33793110dupCGGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000019131.5,