Human SNP ID | rs13273073 |
---|---|
Human chromosome | chr8 |
Human SNP position | 23726713 |
Pig chromosome | chr14 |
Pig SNP position | 8676399 |
PubMed ID | 22310353 |
---|---|
Journal | Pharmacogenomics J |
Link | www.ncbi.nlm.nih.gov/pubmed/22310353 |
Study | Beyond single-marker analyses: mining whole genome scans for insights into treatment responses in severe sepsis. |
Disease/Trait | Treatment response for severe sepsis |
Initial sample | 1,446 individuals |
Replication sample | NA |
Region | 8p21.2 |
Chromosome id | chr8 |
Chromosome position | 23726713 |
Reported gene | NKX2-6 |
Mapped gene | LOC101929258 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101929258 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs13273073-? |
SNPs | rs13273073 |
Merged | 0 |
SNP id current | 13273073 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | (GT vs. not GT) |
Or beta | |
%95 Ci | |
Platform | Illumina [856627] |
CNV | N |
Mapped trait | response to drug |
Mapped trait URI | http://purl.obolibrary.org/obo/GO_0042493 |
Study accession | GCST001402 |