rs37370
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs37370(C;C) |
Make rs37370(C;T) |
Make rs37370(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 35039381 |
Gene | AGXT2 |
is a | snp |
is | mentioned by |
dbSNP | rs37370 |
dbSNP (classic) | rs37370 |
ClinGen | rs37370 |
ebi | rs37370 |
HLI | rs37370 |
Exac | rs37370 |
Gnomad | rs37370 |
Varsome | rs37370 |
LitVar | rs37370 |
Map | rs37370 |
PheGenI | rs37370 |
Biobank | rs37370 |
1000 genomes | rs37370 |
hgdp | rs37370 |
ensembl | rs37370 |
geneview | rs37370 |
scholar | rs37370 |
rs37370 | |
pharmgkb | rs37370 |
gwascentral | rs37370 |
openSNP | rs37370 |
23andMe | rs37370 |
SNPshot | rs37370 |
SNPdbe | rs37370 |
MSV3d | rs37370 |
GWAS Ctlg | rs37370 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24159190] |
Trait | Serum dimethylarginine levels (asymmetric) |
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-7 |
Odds Ratio | .18 [0.12-0.25] unit increase |
[PMID 25620171] Missense variants of the alanine: glyoxylate aminotransferase 2 gene correlated with carotid atherosclerosis in the Japanese population