rs514659
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs514659(A;A) |
Make rs514659(A;C) |
Make rs514659(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 133266790 |
Gene | ABO |
is a | snp |
is | mentioned by |
dbSNP | rs514659 |
dbSNP (classic) | rs514659 |
ClinGen | rs514659 |
ebi | rs514659 |
HLI | rs514659 |
Exac | rs514659 |
Gnomad | rs514659 |
Varsome | rs514659 |
LitVar | rs514659 |
Map | rs514659 |
PheGenI | rs514659 |
Biobank | rs514659 |
1000 genomes | rs514659 |
hgdp | rs514659 |
ensembl | rs514659 |
geneview | rs514659 |
scholar | rs514659 |
rs514659 | |
pharmgkb | rs514659 |
gwascentral | rs514659 |
openSNP | rs514659 |
23andMe | rs514659 |
SNPshot | rs514659 |
SNPdbe | rs514659 |
MSV3d | rs514659 |
GWAS Ctlg | rs514659 |
GMAF | 0.3759 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21239051] |
Trait | |
Title | Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies |
Risk Allele | C |
P-val | 8E-9 |
Odds Ratio | 1.2100 [1.13-1.28] |
[PMID 21343614] Genetic determinants of plasma von Willebrand factor antigen levels: a target gene SNP and haplotype analysis of ARIC cohort.