Human SNP ID | rs7576126 |
---|---|
Human chromosome | chr2 |
Human SNP position | 65431235 |
Pig chromosome | chr3 |
Pig SNP position | 80326323 |
PubMed ID | 26379185 |
---|---|
Journal | PLoS One |
Link | www.ncbi.nlm.nih.gov/pubmed/26379185 |
Study | No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. |
Disease/Trait | Severe influenza A (H1N1) infection |
Initial sample | 49 European ancestry severe cases, 549 European ancestry population controls |
Replication sample | NA |
Region | 2p14 |
Chromosome id | chr2 |
Chromosome position | 65431235 |
Reported gene | SPRED2 |
Mapped gene | SPRED2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 200734 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7576126-? |
SNPs | rs7576126 |
Merged | |
SNP id current | 7576126 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.007576 |
P value | 0.00000000000000002 |
Pvalue mlog | 16.698970004336 |
P value text | |
Or beta | 20.47 |
%95 Ci | [7.811-53.64] |
Platform | Affymetrix [547296] |
CNV | N |
Mapped trait | influenza A (H1N1) |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_1001488 |
Study accession | GCST003123 |