Human SNP ID | rs7094308 |
---|---|
Human chromosome | chr10 |
Human SNP position | 130839042 |
Pig chromosome | chr14 |
Pig SNP position | 151653300 |
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 | Serum dimethylarginine levels (asymmetric/symetric ratio) |
Initial sample | 5110 European ancestry individuals |
Replication sample | NA |
Region | 10q26.3 |
Chromosome id | chr10 |
Chromosome position | 130839042 |
Reported gene | NR |
Mapped gene | LOC105378562 - MIR378C |
Upstream gene id | 105378562 |
Downstream gene id | 100422867 |
SNP gene ids | |
Upstream gene distance | 141990 |
Downstream gene distance | 123546 |
SNP risk allele | rs7094308-T |
SNPs | rs7094308 |
Merged | 0 |
SNP id current | 7094308 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.424 |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | |
Or beta | 0.095 |
%95 Ci | [0.054-0.136] unit decrease |
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 | GCST002242 |