rs137852729
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs137852729(-;C) |
Make rs137852729(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 33302346 |
Gene | CEBPA, CEBPA-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs137852729 |
dbSNP (classic) | rs137852729 |
ClinGen | rs137852729 |
ebi | rs137852729 |
HLI | rs137852729 |
Exac | rs137852729 |
Gnomad | rs137852729 |
Varsome | rs137852729 |
LitVar | rs137852729 |
Map | rs137852729 |
PheGenI | rs137852729 |
Biobank | rs137852729 |
1000 genomes | rs137852729 |
hgdp | rs137852729 |
ensembl | rs137852729 |
geneview | rs137852729 |
scholar | rs137852729 |
rs137852729 | |
pharmgkb | rs137852729 |
gwascentral | rs137852729 |
openSNP | rs137852729 |
23andMe | rs137852729 |
SNPshot | rs137852729 |
SNPdbe | rs137852729 |
MSV3d | rs137852729 |
GWAS Ctlg | rs137852729 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137852729(C;C) |
Alt | rs137852729(C;C) |
Reference | Rs137852729(-;-) |
Significance | Pathogenic |
Disease | Acute myeloid leukemia |
Variation | info |
Gene | CEBPA CEBPA-AS1 |
CLNDBN | Acute myeloid leukemia |
Reversed | 1 |
HGVS | NC_000019.9:g.33793253dupG |
CLNSRC | ClinVar GeneReviews |
CLNACC | RCV000020587.1, |