Human SNP ID | rs275380 |
---|---|
Human chromosome | chr12 |
Human SNP position | 43536193 |
Pig chromosome | chr5 |
Pig SNP position | 77468137 |
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 | 12q12 |
Chromosome id | chr12 |
Chromosome position | 43536193 |
Reported gene | ADAMTS20 |
Mapped gene | ADAMTS20 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 80070 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs275380-? |
SNPs | rs275380 |
Merged | 0 |
SNP id current | 275380 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | (LTG) |
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 |