rs72951640
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs72951640(C;C) |
Make rs72951640(C;T) |
Make rs72951640(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 117524949 |
Gene | LOC105374056 |
is a | snp |
is | mentioned by |
dbSNP | rs72951640 |
dbSNP (classic) | rs72951640 |
ClinGen | rs72951640 |
ebi | rs72951640 |
HLI | rs72951640 |
Exac | rs72951640 |
Gnomad | rs72951640 |
Varsome | rs72951640 |
LitVar | rs72951640 |
Map | rs72951640 |
PheGenI | rs72951640 |
Biobank | rs72951640 |
1000 genomes | rs72951640 |
hgdp | rs72951640 |
ensembl | rs72951640 |
geneview | rs72951640 |
scholar | rs72951640 |
rs72951640 | |
pharmgkb | rs72951640 |
gwascentral | rs72951640 |
openSNP | rs72951640 |
23andMe | rs72951640 |
SNPshot | rs72951640 |
SNPdbe | rs72951640 |
MSV3d | rs72951640 |
GWAS Ctlg | rs72951640 |
Max Magnitude | 0 |
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 | 5E-6 |
Odds Ratio | .41 [0.23-0.58] unit increase |