Human SNP ID | rs6764132 |
---|---|
Human chromosome | chr3 |
Human SNP position | 39747400 |
Pig chromosome | chr13 |
Pig SNP position | 26597160 |
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 | Thrombomodulin 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 | 3p22.1 |
Chromosome id | chr3 |
Chromosome position | 39747400 |
Reported gene | NR |
Mapped gene | NFU1P1 - LOC105377039 |
Upstream gene id | 100132681 |
Downstream gene id | 105377039 |
SNP gene ids | |
Upstream gene distance | 102578 |
Downstream gene distance | 31254 |
SNP risk allele | rs6764132-? |
SNPs | rs6764132 |
Merged | |
SNP id current | 6764132 |
Context | regulatory_region_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.0000009 |
Pvalue mlog | 6.04575749056067 |
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 | GCST003234 |