Human SNP ID | rs1886512 |
---|---|
Human chromosome | chr13 |
Human SNP position | 73946049 |
Pig chromosome | chr11 |
Pig SNP position | 50758382 |
PubMed ID | 21076409 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/21076409 |
Study | Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. |
Disease/Trait | QRS duration |
Initial sample | 39,717 European ancestry individuals, 690 Orcadian individuals |
Replication sample | 7,170 European ancestry individuals |
Region | 13q22.1 |
Chromosome id | chr13 |
Chromosome position | 73946049 |
Reported gene | KLF12 |
Mapped gene | KLF12 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 11278 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1886512-A |
SNPs | rs1886512 |
Merged | 0 |
SNP id current | 1886512 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.37 |
P value | 0.00000001 |
Pvalue mlog | 8 |
P value text | |
Or beta | 0.4 |
%95 Ci | [0.26-0.54] ms decrease |
Platform | Affymetrix, Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | heart function measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004311 |
Study accession | GCST000872 |