rs116875324
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs116875324(C;C) |
Make rs116875324(C;T) |
Make rs116875324(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 121335740 |
is a | snp |
is | mentioned by |
dbSNP | rs116875324 |
dbSNP (classic) | rs116875324 |
ClinGen | rs116875324 |
ebi | rs116875324 |
HLI | rs116875324 |
Exac | rs116875324 |
Gnomad | rs116875324 |
Varsome | rs116875324 |
LitVar | rs116875324 |
Map | rs116875324 |
PheGenI | rs116875324 |
Biobank | rs116875324 |
1000 genomes | rs116875324 |
hgdp | rs116875324 |
ensembl | rs116875324 |
geneview | rs116875324 |
scholar | rs116875324 |
rs116875324 | |
pharmgkb | rs116875324 |
gwascentral | rs116875324 |
openSNP | rs116875324 |
23andMe | rs116875324 |
SNPshot | rs116875324 |
SNPdbe | rs116875324 |
MSV3d | rs116875324 |
GWAS Ctlg | rs116875324 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24159190] |
Trait | Serum dimethylarginine levels (symmetric) |
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 | 9E-6 |
Odds Ratio | .23 [0.13-0.33] unit decrease |