Human SNP ID | rs1426063 |
---|---|
Human chromosome | chr4 |
Human SNP position | 75105711 |
Pig chromosome | chr8 |
Pig SNP position | 75079401 |
PubMed ID | 23166209 |
---|---|
Journal | Circ Cardiovasc Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23166209 |
Study | Impact of ancestry and common genetic variants on QT interval in African Americans. |
Disease/Trait | QT interval |
Initial sample | 13,105 African American individuals |
Replication sample | NA |
Region | 4q13.3 |
Chromosome id | chr4 |
Chromosome position | 75105711 |
Reported gene | NR |
Mapped gene | LOC105377283 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105377283 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1426063-A |
SNPs | rs1426063 |
Merged | 0 |
SNP id current | 1426063 |
Context | downstream_gene_variant |
Intergenic | 0 |
Allele frequency | 0.55 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | |
Or beta | 1.18 |
%95 Ci | [0.67-1.69] unit decrease |
Platform | Affymetrix, Illumina [2800000] (imputed) |
CNV | N |
Mapped trait | QT interval |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004682 |
Study accession | GCST001746 |