rs10519210
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs10519210(G;G) |
Make rs10519210(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 63445726 |
is a | snp |
is | mentioned by |
dbSNP | rs10519210 |
dbSNP (classic) | rs10519210 |
ClinGen | rs10519210 |
ebi | rs10519210 |
HLI | rs10519210 |
Exac | rs10519210 |
Gnomad | rs10519210 |
Varsome | rs10519210 |
LitVar | rs10519210 |
Map | rs10519210 |
PheGenI | rs10519210 |
Biobank | rs10519210 |
1000 genomes | rs10519210 |
hgdp | rs10519210 |
ensembl | rs10519210 |
geneview | rs10519210 |
scholar | rs10519210 |
rs10519210 | |
pharmgkb | rs10519210 |
gwascentral | rs10519210 |
openSNP | rs10519210 |
23andMe | rs10519210 |
SNPshot | rs10519210 |
SNPdbe | rs10519210 |
MSV3d | rs10519210 |
GWAS Ctlg | rs10519210 |
GMAF | 0.06152 |
Max Magnitude | 0 |
? | (G;G) (G;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 | 1E-8 |
Odds Ratio | 1.53 [1.05-2.24] |