Human SNP ID | rs9584669 |
---|---|
Human chromosome | chr13 |
Human SNP position | 97711228 |
Pig chromosome | chr11 |
Pig SNP position | 73987878 |
PubMed ID | 26488411 |
---|---|
Journal | PLoS One |
Link | www.ncbi.nlm.nih.gov/pubmed/26488411 |
Study | Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population. |
Disease/Trait | Peripheral artery disease |
Initial sample | 785 Japanese ancestry cases, 3,383 Japanese ancestry controls |
Replication sample | 2,379 Japanese ancestry cases, 16,752 Japanese ancestry controls |
Region | 13q32.2 |
Chromosome id | chr13 |
Chromosome position | 97711228 |
Reported gene | IPO5, RAP2A |
Mapped gene | LOC105370324 - IPO5 |
Upstream gene id | 105370324 |
Downstream gene id | 3843 |
SNP gene ids | |
Upstream gene distance | 184 |
Downstream gene distance | 242410 |
SNP risk allele | rs9584669-C |
SNPs | rs9584669 |
Merged | |
SNP id current | 9584669 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.00000000000007 |
Pvalue mlog | 13.1549019599857 |
P value text | |
Or beta | 1.72 |
%95 Ci | [1.52-2.00] |
Platform | Illumina [431666] |
CNV | N |
Mapped trait | peripheral arterial disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004265 |
Study accession | GCST003154 |