rs997251
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs997251(A;A) |
Make rs997251(A;G) |
Make rs997251(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 85379684 |
Gene | DDAH1 |
is a | snp |
is | mentioned by |
dbSNP | rs997251 |
dbSNP (classic) | rs997251 |
ClinGen | rs997251 |
ebi | rs997251 |
HLI | rs997251 |
Exac | rs997251 |
Gnomad | rs997251 |
Varsome | rs997251 |
LitVar | rs997251 |
Map | rs997251 |
PheGenI | rs997251 |
Biobank | rs997251 |
1000 genomes | rs997251 |
hgdp | rs997251 |
ensembl | rs997251 |
geneview | rs997251 |
scholar | rs997251 |
rs997251 | |
pharmgkb | rs997251 |
gwascentral | rs997251 |
openSNP | rs997251 |
23andMe | rs997251 |
SNPshot | rs997251 |
SNPdbe | rs997251 |
MSV3d | rs997251 |
GWAS Ctlg | rs997251 |
GMAF | 0.2952 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24159190] Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality