Human SNP ID | rs1915279 |
---|---|
Human chromosome | chr1 |
Human SNP position | 238912414 |
Pig chromosome | chr14 |
Pig SNP position | 56545106 |
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 | 1q43 |
Chromosome id | chr1 |
Chromosome position | 238912414 |
Reported gene | KRT18P32 |
Mapped gene | LOC105373222 - RPL39P10 |
Upstream gene id | 105373222 |
Downstream gene id | 100129952 |
SNP gene ids | |
Upstream gene distance | 64355 |
Downstream gene distance | 140157 |
SNP risk allele | rs1915279-? |
SNPs | rs1915279 |
Merged | 0 |
SNP id current | 1915279 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | (GG vs. not GG) |
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 |