rs10812610
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10812610(A;A) |
Make rs10812610(A;C) |
Make rs10812610(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 27533986 |
is a | snp |
is | mentioned by |
dbSNP | rs10812610 |
dbSNP (classic) | rs10812610 |
ClinGen | rs10812610 |
ebi | rs10812610 |
HLI | rs10812610 |
Exac | rs10812610 |
Gnomad | rs10812610 |
Varsome | rs10812610 |
LitVar | rs10812610 |
Map | rs10812610 |
PheGenI | rs10812610 |
Biobank | rs10812610 |
1000 genomes | rs10812610 |
hgdp | rs10812610 |
ensembl | rs10812610 |
geneview | rs10812610 |
scholar | rs10812610 |
rs10812610 | |
pharmgkb | rs10812610 |
gwascentral | rs10812610 |
openSNP | rs10812610 |
23andMe | rs10812610 |
SNPshot | rs10812610 |
SNPdbe | rs10812610 |
MSV3d | rs10812610 |
GWAS Ctlg | rs10812610 |
GMAF | 0.4807 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 0.000005 |
Odds Ratio | 1.14 [0.99-1.31] |