Human SNP ID | rs7692808 |
---|---|
Human chromosome | chr4 |
Human SNP position | 85719996 |
Pig chromosome | chr8 |
Pig SNP position | 142498330 |
PubMed ID | 20062060 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/20062060 |
Study | Genome-wide association study of PR interval. |
Disease/Trait | PR interval |
Initial sample | 28,517 European ancestry individuals |
Replication sample | NA |
Region | 4q21.23 |
Chromosome id | chr4 |
Chromosome position | 85719996 |
Reported gene | ARHGAP24 |
Mapped gene | ARHGAP24 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 83478 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7692808-A |
SNPs | rs7692808 |
Merged | 0 |
SNP id current | 7692808 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.31 |
P value | 6E-20 |
Pvalue mlog | 19.2218487496163 |
P value text | |
Or beta | 2.01 |
%95 Ci | [1.58-2.44] ms decrease |
Platform | Affymetrix, Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | PR interval |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004462 |
Study accession | GCST000562 |