rs181867028
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs181867028(A;A) |
Make rs181867028(A;T) |
Make rs181867028(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 2541962 |
is a | snp |
is | mentioned by |
dbSNP | rs181867028 |
dbSNP (classic) | rs181867028 |
ClinGen | rs181867028 |
ebi | rs181867028 |
HLI | rs181867028 |
Exac | rs181867028 |
Gnomad | rs181867028 |
Varsome | rs181867028 |
LitVar | rs181867028 |
Map | rs181867028 |
PheGenI | rs181867028 |
Biobank | rs181867028 |
1000 genomes | rs181867028 |
hgdp | rs181867028 |
ensembl | rs181867028 |
geneview | rs181867028 |
scholar | rs181867028 |
rs181867028 | |
pharmgkb | rs181867028 |
gwascentral | rs181867028 |
openSNP | rs181867028 |
23andMe | rs181867028 |
SNPshot | rs181867028 |
SNPdbe | rs181867028 |
MSV3d | rs181867028 |
GWAS Ctlg | rs181867028 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24159190] |
Trait | Serum dimethylarginine levels (asymmetric/symetric ratio) |
Title | Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. |
Risk Allele | T |
P-val | 8E-6 |
Odds Ratio | .91 [0.51-1.31] unit decrease |