Human SNP ID | rs34626661 |
---|---|
Human chromosome | chr2 |
Human SNP position | 222924591 |
Pig chromosome | chr15 |
Pig SNP position | 138699074 |
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 | Mild influenza (H1N1) infection |
Initial sample | 107 European ancestry mild cases, 549 European ancestry population controls |
Replication sample | NA |
Region | 2q36.1 |
Chromosome id | chr2 |
Chromosome position | 222924591 |
Reported gene | ACSL3 |
Mapped gene | ACSL3 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 2181 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs34626661-? |
SNPs | rs34626661 |
Merged | |
SNP id current | 34626661 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0 |
P value | 0.00000002 |
Pvalue mlog | 7.69897000433601 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix [547296] |
CNV | N |
Mapped trait | influenza A (H1N1) |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_1001488 |
Study accession | GCST003124 |