Human SNP ID | rs1505368 |
---|---|
Human chromosome | chr2 |
Human SNP position | 212432529 |
Pig chromosome | chr15 |
Pig SNP position | 127066044 |
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 | 2q34 |
Chromosome id | chr2 |
Chromosome position | 212432529 |
Reported gene | NR |
Mapped gene | ERBB4 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 2066 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1505368-A |
SNPs | rs1505368 |
Merged | 0 |
SNP id current | 1505368 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.509 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 0.097 |
%95 Ci | [0.058-0.136] 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 | GCST002239 |