Human SNP ID | rs4938303 |
---|---|
Human chromosome | chr11 |
Human SNP position | 116714271 |
Pig chromosome | chr9 |
Pig SNP position | 49174617 |
PubMed ID | 20864672 |
---|---|
Journal | Arterioscler Thromb Vasc Biol |
Link | www.ncbi.nlm.nih.gov/pubmed/20864672 |
Study | Genetic variants influencing circulating lipid levels and risk of coronary artery disease. |
Disease/Trait | Triglycerides |
Initial sample | up to 17,723 European ancestry individuals |
Replication sample | up to 37,774 European ancestry individuals, up to 9,665 Indian Asian ancestry individuals |
Region | 11q23.3 |
Chromosome id | chr11 |
Chromosome position | 116714271 |
Reported gene | ZNF259, APOA1, APOC3, APOA4, APOA5, BUD13 |
Mapped gene | LOC101929011 - BUD13 |
Upstream gene id | 101929011 |
Downstream gene id | 84811 |
SNP gene ids | |
Upstream gene distance | 56019 |
Downstream gene distance | 33899 |
SNP risk allele | rs4938303-T |
SNPs | rs4938303 |
Merged | 0 |
SNP id current | 4938303 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.75 |
P value | 4E-21 |
Pvalue mlog | 20.397940008672 |
P value text | |
Or beta | 0.07 |
%95 Ci | [0.06-0.08] unit decrease |
Platform | Affymetrix, Illumina, Perlegen [2155369] (imputed) |
CNV | N |
Mapped trait | triglyceride measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004530 |
Study accession | GCST000809 |