Human SNP ID | rs1042151 |
---|---|
Human chromosome | chr6 |
Human SNP position | 33080884 |
Pig chromosome | chr7 |
Pig SNP position | 29187010 |
PubMed ID | 23180272 |
---|---|
Journal | Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23180272 |
Study | Genome-wide association study of aspirin-exacerbated respiratory disease in a Korean population. |
Disease/Trait | Aspirin exacerbated respiratory disease in asthmatics |
Initial sample | 117 Korean ancestry cases, 685 Korean ancestry controls |
Replication sample | 142 Korean ancestry cases, 996 Korean ancestry controls |
Region | 6p21.32 |
Chromosome id | chr6 |
Chromosome position | 33080884 |
Reported gene | HLA-DPB1 |
Mapped gene | HLA-DPB1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 3115 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1042151-G |
SNPs | rs1042151 |
Merged | 0 |
SNP id current | 1042151 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.083 |
P value | 0.0000005 |
Pvalue mlog | 6.30102999566398 |
P value text | |
Or beta | 2.4 |
%95 Ci | [1.68-3.42] |
Platform | Illumina [430486] |
CNV | N |
Mapped trait | aspirin induced asthma |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0012042 |
Study accession | GCST001747 |