rs113716969
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs113716969(C;C) |
Make rs113716969(C;T) |
Make rs113716969(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 76812369 |
is a | snp |
is | mentioned by |
dbSNP | rs113716969 |
dbSNP (classic) | rs113716969 |
ClinGen | rs113716969 |
ebi | rs113716969 |
HLI | rs113716969 |
Exac | rs113716969 |
Gnomad | rs113716969 |
Varsome | rs113716969 |
LitVar | rs113716969 |
Map | rs113716969 |
PheGenI | rs113716969 |
Biobank | rs113716969 |
1000 genomes | rs113716969 |
hgdp | rs113716969 |
ensembl | rs113716969 |
geneview | rs113716969 |
scholar | rs113716969 |
rs113716969 | |
pharmgkb | rs113716969 |
gwascentral | rs113716969 |
openSNP | rs113716969 |
23andMe | rs113716969 |
SNPshot | rs113716969 |
SNPdbe | rs113716969 |
MSV3d | rs113716969 |
GWAS Ctlg | rs113716969 |
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 | C |
P-val | 2E-6 |
Odds Ratio | .47 [0.28-0.67] unit increase |