Human SNP ID | rs7602460 |
---|---|
Human chromosome | chr2 |
Human SNP position | 181397142 |
Pig chromosome | chr15 |
Pig SNP position | 96478666 |
PubMed ID | 21041692 |
---|---|
Journal | Circulation |
Link | www.ncbi.nlm.nih.gov/pubmed/21041692 |
Study | Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. |
Disease/Trait | Atrioventricular conduction |
Initial sample | 2,334 European ancestry individuals |
Replication sample | NA |
Region | 2q31.3 |
Chromosome id | chr2 |
Chromosome position | 181397142 |
Reported gene | intergenic |
Mapped gene | LOC101927156 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101927156 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7602460-A |
SNPs | rs7602460 |
Merged | 0 |
SNP id current | 7602460 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.4 |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | |
Or beta | 2.42 |
%95 Ci | [1.36-3.48] ms decrease |
Platform | Illumina [514999] |
CNV | N |
Mapped trait | heart function measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004311 |
Study accession | GCST000852 |