rs12034
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs12034(C;C) |
Make rs12034(C;T) |
Make rs12034(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 21 |
Position | 17569905 |
Gene | CXADR |
is a | snp |
is | mentioned by |
dbSNP | rs12034 |
dbSNP (classic) | rs12034 |
ClinGen | rs12034 |
ebi | rs12034 |
HLI | rs12034 |
Exac | rs12034 |
Gnomad | rs12034 |
Varsome | rs12034 |
LitVar | rs12034 |
Map | rs12034 |
PheGenI | rs12034 |
Biobank | rs12034 |
1000 genomes | rs12034 |
hgdp | rs12034 |
ensembl | rs12034 |
geneview | rs12034 |
scholar | rs12034 |
rs12034 | |
pharmgkb | rs12034 |
gwascentral | rs12034 |
openSNP | rs12034 |
23andMe | rs12034 |
SNPshot | rs12034 |
SNPdbe | rs12034 |
MSV3d | rs12034 |
GWAS Ctlg | rs12034 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 29500710] Genome-wide genotype-based risk model for survival in core binding factor acute myeloid leukemia patients.