rs111835151
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs111835151(C;C) |
Make rs111835151(C;G) |
Make rs111835151(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 58974894 |
Gene | LINC01122 |
is a | snp |
is | mentioned by |
dbSNP | rs111835151 |
dbSNP (classic) | rs111835151 |
ClinGen | rs111835151 |
ebi | rs111835151 |
HLI | rs111835151 |
Exac | rs111835151 |
Gnomad | rs111835151 |
Varsome | rs111835151 |
LitVar | rs111835151 |
Map | rs111835151 |
PheGenI | rs111835151 |
Biobank | rs111835151 |
1000 genomes | rs111835151 |
hgdp | rs111835151 |
ensembl | rs111835151 |
geneview | rs111835151 |
scholar | rs111835151 |
rs111835151 | |
pharmgkb | rs111835151 |
gwascentral | rs111835151 |
openSNP | rs111835151 |
23andMe | rs111835151 |
SNPshot | rs111835151 |
SNPdbe | rs111835151 |
MSV3d | rs111835151 |
GWAS Ctlg | rs111835151 |
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 | C |
P-val | 2E-6 |
Odds Ratio | .29 [0.17-0.41] unit decrease |