Human SNP ID | rs1483012 |
---|---|
Human chromosome | chr4 |
Human SNP position | 16892270 |
Pig chromosome | chr8 |
Pig SNP position | 11785711 |
PubMed ID | 23534349 |
---|---|
Journal | Ann Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23534349 |
Study | Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans. |
Disease/Trait | QT interval |
Initial sample | 455 African American individuals |
Replication sample | NA |
Region | 4p15.32 |
Chromosome id | chr4 |
Chromosome position | 16892270 |
Reported gene | LDB2 |
Mapped gene | LDB2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 9079 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1483012-G |
SNPs | rs1483012 |
Merged | 0 |
SNP id current | 1483012 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | |
Or beta | 6.02 |
%95 Ci | [NR] ms increase |
Platform | Illumina [> 930000] |
CNV | N |
Mapped trait | QT interval |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004682 |
Study accession | GCST001922 |