Human SNP ID | rs4569005 |
---|---|
Human chromosome | chr11 |
Human SNP position | 21037185 |
Pig chromosome | chr2 |
Pig SNP position | 41683034 |
PubMed ID | 22379998 |
---|---|
Journal | Pharmacogenomics |
Link | www.ncbi.nlm.nih.gov/pubmed/22379998 |
Study | Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions. |
Disease/Trait | Adverse response to lamotrigine and phenytoin |
Initial sample | 34 European ancestry lamotrigine-induced hypersensitivity cases, 42 European ancestry phenytoin-induced hypersensitivity cases, 1,296 European ancestry controls |
Replication sample | NA |
Region | 11p15.1 |
Chromosome id | chr11 |
Chromosome position | 21037185 |
Reported gene | NELL1 |
Mapped gene | NELL1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4745 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4569005-? |
SNPs | rs4569005 |
Merged | 0 |
SNP id current | 4569005 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | (Total LTG and PHT) |
Or beta | |
%95 Ci | |
Platform | Illumina [NR] |
CNV | N |
Mapped trait | response to anticonvulsant |
Mapped trait URI | http://purl.obolibrary.org/obo/GO_0036277 |
Study accession | GCST001431 |