Human SNP ID | rs10496289 |
---|---|
Human chromosome | chr2 |
Human SNP position | 83066256 |
Pig chromosome | chr3 |
Pig SNP position | 64265830 |
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 | Hypertension |
Initial sample | ~2,000 European ancestry cases, ~3,000 European ancestry controls |
Replication sample | NA |
Region | 2p12 |
Chromosome id | chr2;2 |
Chromosome position | 83065441;83066256 |
Reported gene | intergenic |
Mapped gene | LOC105374832 - LOC105374833; LOC105374832 - LOC105374833 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10496288-G; rs10496289-C |
SNPs | rs10496288; rs10496289 |
Merged | 0 |
SNP id current | |
Context | intergenic_variant; intergenic_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.000000002 |
Pvalue mlog | 8.69897000433601 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix [405022] |
CNV | N |
Mapped trait | hypertension |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000537 |
Study accession | GCST001085 |