rs139419280
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs139419280(A;A) |
Make rs139419280(A;G) |
Make rs139419280(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 82631228 |
Gene | CDH13 |
is a | snp |
is | mentioned by |
dbSNP | rs139419280 |
dbSNP (classic) | rs139419280 |
ClinGen | rs139419280 |
ebi | rs139419280 |
HLI | rs139419280 |
Exac | rs139419280 |
Gnomad | rs139419280 |
Varsome | rs139419280 |
LitVar | rs139419280 |
Map | rs139419280 |
PheGenI | rs139419280 |
Biobank | rs139419280 |
1000 genomes | rs139419280 |
hgdp | rs139419280 |
ensembl | rs139419280 |
geneview | rs139419280 |
scholar | rs139419280 |
rs139419280 | |
pharmgkb | rs139419280 |
gwascentral | rs139419280 |
openSNP | rs139419280 |
23andMe | rs139419280 |
SNPshot | rs139419280 |
SNPdbe | rs139419280 |
MSV3d | rs139419280 |
GWAS Ctlg | rs139419280 |
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 | G |
P-val | 8E-6 |
Odds Ratio | 1.99 [1.11-2.86] unit increase |