Human SNP ID | rs61361928 |
---|---|
Human chromosome | chr4 |
Human SNP position | 69096657 |
Pig chromosome | chr8 |
Pig SNP position | 70585194 |
PubMed ID | 25935875 |
---|---|
Journal | Eur Heart J |
Link | www.ncbi.nlm.nih.gov/pubmed/25935875 |
Study | Effect of genetic variations on ticagrelor plasma levels and clinical outcomes. |
Disease/Trait | AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor |
Initial sample | 1,794 European ancestry cases, 18 African and Asian ancestry cases |
Replication sample | 1,922 European ancestry cases, 19 African and Asian ancestry cases |
Region | 4q13.2 |
Chromosome id | chr4 |
Chromosome position | 69096657 |
Reported gene | UGT2B7 |
Mapped gene | UGT2B7 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 7364 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs61361928-T |
SNPs | rs61361928 |
Merged | 0 |
SNP id current | 61361928 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.005 |
P value | 0.00000000000008 |
Pvalue mlog | 13.096910013008 |
P value text | |
Or beta | 0.385 |
%95 Ci | [0.29-0.48] unit increase |
Platform | Illumina [10962468] (imputed) |
CNV | N |
Mapped trait | AR-C124910XX�measurement, acute coronary syndrome |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0007020, http://www.ebi.ac.uk/efo/EFO_0005672 |
Study accession | GCST002883 |