rs1884139
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1884139(G;G) |
Make rs1884139(G;T) |
Make rs1884139(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 85380315 |
Gene | DDAH1 |
is a | snp |
is | mentioned by |
dbSNP | rs1884139 |
dbSNP (classic) | rs1884139 |
ClinGen | rs1884139 |
ebi | rs1884139 |
HLI | rs1884139 |
Exac | rs1884139 |
Gnomad | rs1884139 |
Varsome | rs1884139 |
LitVar | rs1884139 |
Map | rs1884139 |
PheGenI | rs1884139 |
Biobank | rs1884139 |
1000 genomes | rs1884139 |
hgdp | rs1884139 |
ensembl | rs1884139 |
geneview | rs1884139 |
scholar | rs1884139 |
rs1884139 | |
pharmgkb | rs1884139 |
gwascentral | rs1884139 |
openSNP | rs1884139 |
23andMe | rs1884139 |
SNPshot | rs1884139 |
SNPdbe | rs1884139 |
MSV3d | rs1884139 |
GWAS Ctlg | rs1884139 |
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 | 1E-18 |
Odds Ratio | .18 [0.14-0.22] unit decrease |