Human SNP ID | rs28377390 |
---|---|
Human chromosome | chr15 |
Human SNP position | 97197508 |
Pig chromosome | chr7 |
Pig SNP position | 88206867 |
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 | 15q26.2 |
Chromosome id | chr15 |
Chromosome position | 97197508 |
Reported gene | LOC101927286, SPATA8 |
Mapped gene | LOC105371005 - LOC105371006 |
Upstream gene id | 105371005 |
Downstream gene id | 105371006 |
SNP gene ids | |
Upstream gene distance | 78362 |
Downstream gene distance | 74701 |
SNP risk allele | rs28377390-? |
SNPs | rs28377390 |
Merged | |
SNP id current | 28377390 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.007407 |
P value | 0.000000000004 |
Pvalue mlog | 11.397940008672 |
P value text | |
Or beta | 15.31 |
%95 Ci | [5.581-42.02] |
Platform | Affymetrix [547296] |
CNV | N |
Mapped trait | influenza A (H1N1) |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_1001488 |
Study accession | GCST003123 |