rs191493117
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs191493117(C;C) |
Make rs191493117(C;T) |
Make rs191493117(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 146438979 |
Gene | SLC10A7 |
is a | snp |
is | mentioned by |
dbSNP | rs191493117 |
dbSNP (classic) | rs191493117 |
ClinGen | rs191493117 |
ebi | rs191493117 |
HLI | rs191493117 |
Exac | rs191493117 |
Gnomad | rs191493117 |
Varsome | rs191493117 |
LitVar | rs191493117 |
Map | rs191493117 |
PheGenI | rs191493117 |
Biobank | rs191493117 |
1000 genomes | rs191493117 |
hgdp | rs191493117 |
ensembl | rs191493117 |
geneview | rs191493117 |
scholar | rs191493117 |
rs191493117 | |
pharmgkb | rs191493117 |
gwascentral | rs191493117 |
openSNP | rs191493117 |
23andMe | rs191493117 |
SNPshot | rs191493117 |
SNPdbe | rs191493117 |
MSV3d | rs191493117 |
GWAS Ctlg | rs191493117 |
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 | 3E-6 |
Odds Ratio | 2.06 [1.2-2.92] unit decrease |