rs10418356
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10418356(C;C) |
Make rs10418356(C;G) |
Make rs10418356(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 30544779 |
Gene | ZNF536 |
is a | snp |
is | mentioned by |
dbSNP | rs10418356 |
dbSNP (classic) | rs10418356 |
ClinGen | rs10418356 |
ebi | rs10418356 |
HLI | rs10418356 |
Exac | rs10418356 |
Gnomad | rs10418356 |
Varsome | rs10418356 |
LitVar | rs10418356 |
Map | rs10418356 |
PheGenI | rs10418356 |
Biobank | rs10418356 |
1000 genomes | rs10418356 |
hgdp | rs10418356 |
ensembl | rs10418356 |
geneview | rs10418356 |
scholar | rs10418356 |
rs10418356 | |
pharmgkb | rs10418356 |
gwascentral | rs10418356 |
openSNP | rs10418356 |
23andMe | rs10418356 |
SNPshot | rs10418356 |
SNPdbe | rs10418356 |
MSV3d | rs10418356 |
GWAS Ctlg | rs10418356 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 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 | G |
P-val | 7E-6 |
Odds Ratio | .26 [0.15-0.37] unit increase |