Human SNP ID | rs602633 |
---|---|
Human chromosome | chr1 |
Human SNP position | 109278889 |
Pig chromosome | chr4 |
Pig SNP position | 121297709 |
PubMed ID | 24262325 |
---|---|
Journal | Stroke |
Link | www.ncbi.nlm.nih.gov/pubmed/24262325 |
Study | Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. |
Disease/Trait | Coronary artery disease |
Initial sample | 33,398 cases, 75,726 controls |
Replication sample | NA |
Region | 1p13.3 |
Chromosome id | chr1 |
Chromosome position | 109278889 |
Reported gene | SORT1 |
Mapped gene | CELSR2 - PSRC1 |
Upstream gene id | 1952 |
Downstream gene id | 84722 |
SNP gene ids | |
Upstream gene distance | 3133 |
Downstream gene distance | 665 |
SNP risk allele | rs602633-T |
SNPs | rs602633 |
Merged | 0 |
SNP id current | 602633 |
Context | downstream_gene_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.00000001 |
Pvalue mlog | 8 |
P value text | |
Or beta | 1.1111 |
%95 Ci | [1.08-1.15] |
Platform | Illumina [575000] (imputed) |
CNV | N |
Mapped trait | coronary heart disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001645 |
Study accession | GCST002289 |