Human SNP ID | rs11465699 |
---|---|
Human chromosome | chr2 |
Human SNP position | 102438307 |
Pig chromosome | chr3 |
Pig SNP position | 54257787 |
PubMed ID | 23999434 |
---|---|
Journal | J Clin Invest |
Link | www.ncbi.nlm.nih.gov/pubmed/23999434 |
Study | Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling. |
Disease/Trait | Serum protein levels (sST2) |
Initial sample | 2,797 individuals |
Replication sample | NA |
Region | 2q12.1 |
Chromosome id | chr2 |
Chromosome position | 102438307 |
Reported gene | IL18RAP |
Mapped gene | IL18RAP |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 8807 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11465699-A |
SNPs | rs11465699 |
Merged | 0 |
SNP id current | 11465699 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.06 |
P value | 0.00000002 |
Pvalue mlog | 7.69897000433601 |
P value text | |
Or beta | 0.14 |
%95 Ci | [0.1-0.18] unit increase |
Platform | Affymetrix [2500000] (imputed) |
CNV | N |
Mapped trait | serum ST2 measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005416 |
Study accession | GCST002166 |