Human SNP ID | rs6455 |
---|---|
Human chromosome | chr6 |
Human SNP position | 32039119 |
Pig chromosome | chr7 |
Pig SNP position | 27725329 |
PubMed ID | 26385043 |
---|---|
Journal | Am Heart J |
Link | www.ncbi.nlm.nih.gov/pubmed/26385043 |
Study | Genome-wide association study of new-onset atrial fibrillation after coronary artery bypass grafting surgery. |
Disease/Trait | Postoperative atrial fibrillation in coronary artery bypass grafting surgery |
Initial sample | 620 European ancestry cases, 257 European ancestry controls |
Replication sample | 220 cases, 84 controls |
Region | 6p21.33 |
Chromosome id | chr6 |
Chromosome position | 32039119 |
Reported gene | CYP21A2 |
Mapped gene | CYP21A2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1589 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6455-G |
SNPs | rs6455 |
Merged | |
SNP id current | 6455 |
Context | synonymous_variant |
Intergenic | 0 |
Allele frequency | 0.015 |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | |
Or beta | 1.96 |
%95 Ci | [0.51-7.58] |
Platform | Illumina [524975] |
CNV | N |
Mapped trait | coronary artery bypass, atrial fibrillation |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003776, http://www.ebi.ac.uk/efo/EFO_0000275 |
Study accession | GCST002975 |