rs17019682
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs17019682(A;T) |
Make rs17019682(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 91911494 |
is a | snp |
is | mentioned by |
dbSNP | rs17019682 |
dbSNP (classic) | rs17019682 |
ClinGen | rs17019682 |
ebi | rs17019682 |
HLI | rs17019682 |
Exac | rs17019682 |
Gnomad | rs17019682 |
Varsome | rs17019682 |
LitVar | rs17019682 |
Map | rs17019682 |
PheGenI | rs17019682 |
Biobank | rs17019682 |
1000 genomes | rs17019682 |
hgdp | rs17019682 |
ensembl | rs17019682 |
geneview | rs17019682 |
scholar | rs17019682 |
rs17019682 | |
pharmgkb | rs17019682 |
gwascentral | rs17019682 |
openSNP | rs17019682 |
23andMe | rs17019682 |
SNPshot | rs17019682 |
SNPdbe | rs17019682 |
MSV3d | rs17019682 |
GWAS Ctlg | rs17019682 |
GMAF | 0.06566 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20445134] |
Trait | Heart failure |
Title | The Association of Genome-Wide Variation with the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis from the CHARGE Consortium |
Risk Allele | |
P-val | 0.000002 |
Odds Ratio | 1.47 [0.98-2.22] |