rs13418717
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs13418717(A;A) |
Make rs13418717(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 126905321 |
is a | snp |
is | mentioned by |
dbSNP | rs13418717 |
dbSNP (classic) | rs13418717 |
ClinGen | rs13418717 |
ebi | rs13418717 |
HLI | rs13418717 |
Exac | rs13418717 |
Gnomad | rs13418717 |
Varsome | rs13418717 |
LitVar | rs13418717 |
Map | rs13418717 |
PheGenI | rs13418717 |
Biobank | rs13418717 |
1000 genomes | rs13418717 |
hgdp | rs13418717 |
ensembl | rs13418717 |
geneview | rs13418717 |
scholar | rs13418717 |
rs13418717 | |
pharmgkb | rs13418717 |
gwascentral | rs13418717 |
openSNP | rs13418717 |
23andMe | rs13418717 |
SNPshot | rs13418717 |
SNPdbe | rs13418717 |
MSV3d | rs13418717 |
GWAS Ctlg | rs13418717 |
GMAF | 0.1331 |
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 | 0.000003 |
Odds Ratio | 1.46 [0.97-2.20] |