rs4862307
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4862307(A;A) |
Make rs4862307(A;T) |
Make rs4862307(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 184086240 |
is a | snp |
is | mentioned by |
dbSNP | rs4862307 |
dbSNP (classic) | rs4862307 |
ClinGen | rs4862307 |
ebi | rs4862307 |
HLI | rs4862307 |
Exac | rs4862307 |
Gnomad | rs4862307 |
Varsome | rs4862307 |
LitVar | rs4862307 |
Map | rs4862307 |
PheGenI | rs4862307 |
Biobank | rs4862307 |
1000 genomes | rs4862307 |
hgdp | rs4862307 |
ensembl | rs4862307 |
geneview | rs4862307 |
scholar | rs4862307 |
rs4862307 | |
pharmgkb | rs4862307 |
gwascentral | rs4862307 |
openSNP | rs4862307 |
23andMe | rs4862307 |
SNPshot | rs4862307 |
SNPdbe | rs4862307 |
MSV3d | rs4862307 |
GWAS Ctlg | rs4862307 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
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 | 6E-6 |
Odds Ratio | .10 [0.055-0.141] unit decrease |