Human SNP ID | rs4884502 |
---|---|
Human chromosome | chr13 |
Human SNP position | 63636265 |
Pig chromosome | chr11 |
Pig SNP position | 38633655 |
PubMed ID | 24792382 |
---|---|
Journal | Clin Chim Acta |
Link | www.ncbi.nlm.nih.gov/pubmed/24792382 |
Study | Genome-wide association study identifies ALLC polymorphisms correlated with FEV₁ change by corticosteroid. |
Disease/Trait | Response to inhaled corticosteroid treatment in asthma (percentage change of FEV1) |
Initial sample | 189 Korean ancestry cases |
Replication sample | NA |
Region | 13q21.31 |
Chromosome id | chr13 |
Chromosome position | 63636265 |
Reported gene | OR7E156P |
Mapped gene | LOC105370236 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105370236 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4884502-? |
SNPs | rs4884502 |
Merged | 0 |
SNP id current | 4884502 |
Context | regulatory_region_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000009 |
Pvalue mlog | 5.04575749056067 |
P value text | |
Or beta | 0.32 |
%95 Ci | [NR] unit increase |
Platform | Illumina [430487] |
CNV | N |
Mapped trait | FEV change measurement, response to corticosteroid, asthma |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005921, http://purl.obolibrary.org/obo/GO_0031960, http://www.ebi.ac.uk/efo/EFO_0000270 |
Study accession | GCST002432 |