rs7088627
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7088627(A;A) |
Make rs7088627(A;T) |
Make rs7088627(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 61432656 |
Gene | TMEM26 |
is a | snp |
is | mentioned by |
dbSNP | rs7088627 |
dbSNP (classic) | rs7088627 |
ClinGen | rs7088627 |
ebi | rs7088627 |
HLI | rs7088627 |
Exac | rs7088627 |
Gnomad | rs7088627 |
Varsome | rs7088627 |
LitVar | rs7088627 |
Map | rs7088627 |
PheGenI | rs7088627 |
Biobank | rs7088627 |
1000 genomes | rs7088627 |
hgdp | rs7088627 |
ensembl | rs7088627 |
geneview | rs7088627 |
scholar | rs7088627 |
rs7088627 | |
pharmgkb | rs7088627 |
gwascentral | rs7088627 |
openSNP | rs7088627 |
23andMe | rs7088627 |
SNPshot | rs7088627 |
SNPdbe | rs7088627 |
MSV3d | rs7088627 |
GWAS Ctlg | rs7088627 |
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 | A |
P-val | 7E-6 |
Odds Ratio | .11 [0.061-0.151] unit increase |