Human SNP ID | rs783396 |
---|---|
Human chromosome | chr6 |
Human SNP position | 106539495 |
Pig chromosome | chr1 |
Pig SNP position | 82029850 |
PubMed ID | 17434096 |
---|---|
Journal | Lancet Neurol |
Link | www.ncbi.nlm.nih.gov/pubmed/17434096 |
Study | A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. |
Disease/Trait | Stroke |
Initial sample | 259 European ancestry cases, 269 European ancestry controls |
Replication sample | NA |
Region | 6q21 |
Chromosome id | chr6 |
Chromosome position | 106539495 |
Reported gene | AIM1 |
Mapped gene | AIM1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 202 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs783396-? |
SNPs | rs783396 |
Merged | 0 |
SNP id current | 783396 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.9 |
P value | 0.000009 |
Pvalue mlog | 5.04575749056067 |
P value text | |
Or beta | 2.17 |
%95 Ci | [1.47-3.13] |
Platform | Illumina [408803] |
CNV | N |
Mapped trait | stroke |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000712 |
Study accession | GCST000032 |