rs11172782
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs11172782(A;G) |
Make rs11172782(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 58865846 |
is a | snp |
is | mentioned by |
dbSNP | rs11172782 |
dbSNP (classic) | rs11172782 |
ClinGen | rs11172782 |
ebi | rs11172782 |
HLI | rs11172782 |
Exac | rs11172782 |
Gnomad | rs11172782 |
Varsome | rs11172782 |
LitVar | rs11172782 |
Map | rs11172782 |
PheGenI | rs11172782 |
Biobank | rs11172782 |
1000 genomes | rs11172782 |
hgdp | rs11172782 |
ensembl | rs11172782 |
geneview | rs11172782 |
scholar | rs11172782 |
rs11172782 | |
pharmgkb | rs11172782 |
gwascentral | rs11172782 |
openSNP | rs11172782 |
23andMe | rs11172782 |
SNPshot | rs11172782 |
SNPdbe | rs11172782 |
MSV3d | rs11172782 |
GWAS Ctlg | rs11172782 |
GMAF | 0.1244 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 7E-8 |
Odds Ratio | 1.46 [1.03-2.09] |