Human SNP ID | rs749141 |
---|---|
Human chromosome | chr10 |
Human SNP position | 128571226 |
Pig chromosome | chr14 |
Pig SNP position | 149560885 |
PubMed ID | 24159190 |
---|---|
Journal | Eur Heart J |
Link | www.ncbi.nlm.nih.gov/pubmed/24159190 |
Study | Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. |
Disease/Trait | Symmetrical dimethylarginine levels |
Initial sample | 5110 European ancestry individuals |
Replication sample | NA |
Region | 10q26.2 |
Chromosome id | chr10 |
Chromosome position | 128571226 |
Reported gene | NR |
Mapped gene | LINC01163 - LOC105378554 |
Upstream gene id | 101927381 |
Downstream gene id | 105378554 |
SNP gene ids | |
Upstream gene distance | 253500 |
Downstream gene distance | 114178 |
SNP risk allele | rs749141-C |
SNPs | rs749141 |
Merged | 0 |
SNP id current | 749141 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.076 |
P value | 0.0000004 |
Pvalue mlog | 6.39794000867203 |
P value text | |
Or beta | 0.196 |
%95 Ci | [0.12-0.27] unit increase |
Platform | Affymetrix, Illumina [10085758] (imputed) |
CNV | N |
Mapped trait | serum dimethylarginine measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005418 |
Study accession | GCST002239 |