Human SNP ID | rs148359873 |
---|---|
Human chromosome | chr9 |
Human SNP position | 31450668 |
Pig chromosome | chr10 |
Pig SNP position | 39261329 |
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 | 9p21.1 |
Chromosome id | chr9 |
Chromosome position | 31450668 |
Reported gene | NR |
Mapped gene | LINC01243 - LOC105376010 |
Upstream gene id | 101929620 |
Downstream gene id | 105376010 |
SNP gene ids | |
Upstream gene distance | 69178 |
Downstream gene distance | 127950 |
SNP risk allele | rs148359873-T |
SNPs | rs148359873 |
Merged | 0 |
SNP id current | 148359873 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.03 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | 0.342 |
%95 Ci | [0.2-0.49] 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 |
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 | 9p21.1 |
Chromosome id | chr9 |
Chromosome position | 31450668 |
Reported gene | NR |
Mapped gene | LINC01243 - LOC105376010 |
Upstream gene id | 101929620 |
Downstream gene id | 105376010 |
SNP gene ids | |
Upstream gene distance | 69178 |
Downstream gene distance | 127950 |
SNP risk allele | rs148359873-T |
SNPs | rs148359873 |
Merged | 0 |
SNP id current | 148359873 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.03 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 0.361 |
%95 Ci | [0.21-0.51] 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 |