rs115426111
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs115426111(A;A) |
Make rs115426111(A;T) |
Make rs115426111(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 38159443 |
is a | snp |
is | mentioned by |
dbSNP | rs115426111 |
dbSNP (classic) | rs115426111 |
ClinGen | rs115426111 |
ebi | rs115426111 |
HLI | rs115426111 |
Exac | rs115426111 |
Gnomad | rs115426111 |
Varsome | rs115426111 |
LitVar | rs115426111 |
Map | rs115426111 |
PheGenI | rs115426111 |
Biobank | rs115426111 |
1000 genomes | rs115426111 |
hgdp | rs115426111 |
ensembl | rs115426111 |
geneview | rs115426111 |
scholar | rs115426111 |
rs115426111 | |
pharmgkb | rs115426111 |
gwascentral | rs115426111 |
openSNP | rs115426111 |
23andMe | rs115426111 |
SNPshot | rs115426111 |
SNPdbe | rs115426111 |
MSV3d | rs115426111 |
GWAS Ctlg | rs115426111 |
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 | 7E-6 |
Odds Ratio | 1.40 [0.79-2.01] unit increase |