rs148359873
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs148359873(C;C) |
Make rs148359873(C;T) |
Make rs148359873(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 31450668 |
is a | snp |
is | mentioned by |
dbSNP | rs148359873 |
dbSNP (classic) | rs148359873 |
ClinGen | rs148359873 |
ebi | rs148359873 |
HLI | rs148359873 |
Exac | rs148359873 |
Gnomad | rs148359873 |
Varsome | rs148359873 |
LitVar | rs148359873 |
Map | rs148359873 |
PheGenI | rs148359873 |
Biobank | rs148359873 |
1000 genomes | rs148359873 |
hgdp | rs148359873 |
ensembl | rs148359873 |
geneview | rs148359873 |
scholar | rs148359873 |
rs148359873 | |
pharmgkb | rs148359873 |
gwascentral | rs148359873 |
openSNP | rs148359873 |
23andMe | rs148359873 |
SNPshot | rs148359873 |
SNPdbe | rs148359873 |
MSV3d | rs148359873 |
GWAS Ctlg | rs148359873 |
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 | 5E-6 |
Odds Ratio | .34 [0.2-0.49] unit decrease |