rs78192384
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs78192384(A;A) |
Make rs78192384(A;G) |
Make rs78192384(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 3041399 |
is a | snp |
is | mentioned by |
dbSNP | rs78192384 |
dbSNP (classic) | rs78192384 |
ClinGen | rs78192384 |
ebi | rs78192384 |
HLI | rs78192384 |
Exac | rs78192384 |
Gnomad | rs78192384 |
Varsome | rs78192384 |
LitVar | rs78192384 |
Map | rs78192384 |
PheGenI | rs78192384 |
Biobank | rs78192384 |
1000 genomes | rs78192384 |
hgdp | rs78192384 |
ensembl | rs78192384 |
geneview | rs78192384 |
scholar | rs78192384 |
rs78192384 | |
pharmgkb | rs78192384 |
gwascentral | rs78192384 |
openSNP | rs78192384 |
23andMe | rs78192384 |
SNPshot | rs78192384 |
SNPdbe | rs78192384 |
MSV3d | rs78192384 |
GWAS Ctlg | rs78192384 |
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 | A |
P-val | 7E-6 |
Odds Ratio | .27 [0.15-0.39] unit decrease |