Human SNP ID | rs899997 |
---|---|
Human chromosome | chr15 |
Human SNP position | 78727236 |
Pig chromosome | chr1 |
Pig SNP position | 302710371 |
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 or large artery stroke |
Initial sample | 2,167 Large artery stroke cases, 22,233 Coronary artery disease cases, ~ 75,921 controls |
Replication sample | NA |
Region | 15q25.1 |
Chromosome id | chr15 |
Chromosome position | 78727236 |
Reported gene | ADAMTS7 |
Mapped gene | LOC105370913 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105370913 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs899997-? |
SNPs | rs899997 |
Merged | 0 |
SNP id current | 899997 |
Context | non_coding_transcript_exon_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.00000002 |
Pvalue mlog | 7.69897000433601 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix, Illumina [up to 2500000] (imputed) |
CNV | N |
Mapped trait | large artery stroke, coronary heart disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005524, http://www.ebi.ac.uk/efo/EFO_0001645 |
Study accession | GCST002290 |