Human SNP ID | rs16912059 |
---|---|
Human chromosome | chr11 |
Human SNP position | 24069597 |
Pig chromosome | chr2 |
Pig SNP position | 38591472 |
PubMed ID | 26718567 |
---|---|
Journal | Neurology |
Link | www.ncbi.nlm.nih.gov/pubmed/26718567 |
Study | Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke. |
Disease/Trait | Thrombin-antithrombin complex levels in ischemic stroke |
Initial sample | up to 1,725 European ancestry cases, up to 258 African ancestry cases, up to 117 cases |
Replication sample | NA |
Region | 11p14.3 |
Chromosome id | chr11 |
Chromosome position | 24069597 |
Reported gene | NR |
Mapped gene | LOC105376593 - LOC105376594 |
Upstream gene id | 105376593 |
Downstream gene id | 105376594 |
SNP gene ids | |
Upstream gene distance | 319679 |
Downstream gene distance | 189788 |
SNP risk allele | rs16912059-? |
SNPs | rs16912059 |
Merged | |
SNP id current | 16912059 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [7500450] (imputed) |
CNV | N |
Mapped trait | Ischemic stroke |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0002140 |
Study accession | GCST003233 |