Human SNP ID | rs11924705 |
---|---|
Human chromosome | chr3 |
Human SNP position | 162443828 |
Pig chromosome | chr13 |
Pig SNP position | 110455119 |
PubMed ID | 21626137 |
---|---|
Journal | Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/21626137 |
Study | Two-marker association tests yield new disease associations for coronary artery disease and hypertension. |
Disease/Trait | Coronary heart disease |
Initial sample | ~2,000 European ancestry cases, ~3,000 European ancestry controls |
Replication sample | NA |
Region | 3q26.1 |
Chromosome id | chr3;3 |
Chromosome position | 162443828;162449608 |
Reported gene | intergenic |
Mapped gene | OTOL1 - LINC01192; OTOL1 - LINC01192 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11924705-C; rs6789378-A |
SNPs | rs11924705; rs6789378 |
Merged | 0 |
SNP id current | |
Context | intergenic_variant; intergenic_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.00000000000004 |
Pvalue mlog | 13.397940008672 |
P value text | (Coronary artery disease) |
Or beta | |
%95 Ci | |
Platform | Affymetrix [407576] |
CNV | N |
Mapped trait | coronary heart disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001645 |
Study accession | GCST001084 |