rs8017423
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8017423(C;C) |
Make rs8017423(C;T) |
Make rs8017423(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 90213566 |
is a | snp |
is | mentioned by |
dbSNP | rs8017423 |
dbSNP (classic) | rs8017423 |
ClinGen | rs8017423 |
ebi | rs8017423 |
HLI | rs8017423 |
Exac | rs8017423 |
Gnomad | rs8017423 |
Varsome | rs8017423 |
LitVar | rs8017423 |
Map | rs8017423 |
PheGenI | rs8017423 |
Biobank | rs8017423 |
1000 genomes | rs8017423 |
hgdp | rs8017423 |
ensembl | rs8017423 |
geneview | rs8017423 |
scholar | rs8017423 |
rs8017423 | |
pharmgkb | rs8017423 |
gwascentral | rs8017423 |
openSNP | rs8017423 |
23andMe | rs8017423 |
SNPshot | rs8017423 |
SNPdbe | rs8017423 |
MSV3d | rs8017423 |
GWAS Ctlg | rs8017423 |
GMAF | 0.5 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20400778] |
Trait | Mortality among heart failure patients |
Title | Genomic Variation Associated with Mortality among Adults of European and African Ancestry with Heart Failure: The CHARGE Consortium |
Risk Allele | T |
P-val | 0.000007 |
Odds Ratio | 1.64 [0.94-2.78] |