rs117147010
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs117147010(C;C) |
Make rs117147010(C;T) |
Make rs117147010(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 12503078 |
Gene | SNX29 |
is a | snp |
is | mentioned by |
dbSNP | rs117147010 |
dbSNP (classic) | rs117147010 |
ClinGen | rs117147010 |
ebi | rs117147010 |
HLI | rs117147010 |
Exac | rs117147010 |
Gnomad | rs117147010 |
Varsome | rs117147010 |
LitVar | rs117147010 |
Map | rs117147010 |
PheGenI | rs117147010 |
Biobank | rs117147010 |
1000 genomes | rs117147010 |
hgdp | rs117147010 |
ensembl | rs117147010 |
geneview | rs117147010 |
scholar | rs117147010 |
rs117147010 | |
pharmgkb | rs117147010 |
gwascentral | rs117147010 |
openSNP | rs117147010 |
23andMe | rs117147010 |
SNPshot | rs117147010 |
SNPdbe | rs117147010 |
MSV3d | rs117147010 |
GWAS Ctlg | rs117147010 |
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 | .35 [0.2-0.49] unit increase |