Human SNP ID | rs6445035 |
---|---|
Human chromosome | chr3 |
Human SNP position | 165762312 |
Pig chromosome | chr13 |
Pig SNP position | 113407996 |
PubMed ID | 23508960 |
---|---|
Journal | J Biol Chem |
Link | www.ncbi.nlm.nih.gov/pubmed/23508960 |
Study | Aspirin hydrolysis in plasma is a variable function of butyrylcholinesterase and platelet-activating factor acetylhydrolase 1b2 (PAFAH1b2). |
Disease/Trait | Aspirin hydrolysis (plasma) |
Initial sample | 2,054 European ancestry individuals |
Replication sample | |
Region | 3q26.1 |
Chromosome id | chr3 |
Chromosome position | 165762312 |
Reported gene | BCHE |
Mapped gene | LINC01322 - BCHE |
Upstream gene id | 103695433 |
Downstream gene id | 590 |
SNP gene ids | |
Upstream gene distance | 248584 |
Downstream gene distance | 10592 |
SNP risk allele | rs6445035-A |
SNPs | rs6445035 |
Merged | 0 |
SNP id current | 6445035 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.00000000000000009 |
Pvalue mlog | 16.0457574905606 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix [2421779] (imputed) |
CNV | N |
Mapped trait | aspirin hydrolysis measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005211 |
Study accession | GCST001910 |