rs181715218
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs181715218(C;C) |
Make rs181715218(C;T) |
Make rs181715218(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 79425558 |
Gene | ZCCHC24 |
is a | snp |
is | mentioned by |
dbSNP | rs181715218 |
dbSNP (classic) | rs181715218 |
ClinGen | rs181715218 |
ebi | rs181715218 |
HLI | rs181715218 |
Exac | rs181715218 |
Gnomad | rs181715218 |
Varsome | rs181715218 |
LitVar | rs181715218 |
Map | rs181715218 |
PheGenI | rs181715218 |
Biobank | rs181715218 |
1000 genomes | rs181715218 |
hgdp | rs181715218 |
ensembl | rs181715218 |
geneview | rs181715218 |
scholar | rs181715218 |
rs181715218 | |
pharmgkb | rs181715218 |
gwascentral | rs181715218 |
openSNP | rs181715218 |
23andMe | rs181715218 |
SNPshot | rs181715218 |
SNPdbe | rs181715218 |
MSV3d | rs181715218 |
GWAS Ctlg | rs181715218 |
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 | T |
P-val | 3E-6 |
Odds Ratio | 1.30 [0.76-1.84] unit decrease |