Have questions? Visit https://www.reddit.com/r/SNPedia

rs121912791

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912791(G;T)
Make rs121912791(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position33302267
GeneCEBPA
is asnp
is mentioned by
dbSNPrs121912791
ebirs121912791
HLIrs121912791
Exacrs121912791
Varsomers121912791
Maprs121912791
PheGenIrs121912791
hapmaprs121912791
1000 genomesrs121912791
hgdprs121912791
ensemblrs121912791
gopubmedrs121912791
geneviewrs121912791
scholarrs121912791
googlers121912791
pharmgkbrs121912791
gwascentralrs121912791
openSNPrs121912791
23andMers121912791
23andMe allrs121912791
SNP Nexus

SNPshotrs121912791
SNPdbers121912791
MSV3drs121912791
GWAS Ctlgrs121912791
Max Magnitude0
OMIM116897
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912791(T;T)
Alt rs121912791(T;T)
Reference rs121912791(G;G)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene CEBPA CEBPA-AS1
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000019.9:g.33793173C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019127.5,