Human SNP ID | rs1937332 |
---|---|
Human chromosome | chr10 |
Human SNP position | 89067022 |
Pig chromosome | chr14 |
Pig SNP position | 109973706 |
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 | 10q23.31 |
Chromosome id | chr10 |
Chromosome position | 89067022 |
Reported gene | CH25H, FAS |
Mapped gene | MIR4679-2 - LOC105378418 |
Upstream gene id | 100616192 |
Downstream gene id | 105378418 |
SNP gene ids | |
Upstream gene distance | 3611 |
Downstream gene distance | 112280 |
SNP risk allele | rs1937332-G |
SNPs | rs1937332 |
Merged | 0 |
SNP id current | 1937332 |
Context | upstream_gene_variant |
Intergenic | 1 |
Allele frequency | 0.47 |
P value | 0.0000007 |
Pvalue mlog | 6.15490195998574 |
P value text | |
Or beta | 2.6 |
%95 Ci | [1.58-3.62] ms increase |
Platform | Illumina [514999] |
CNV | N |
Mapped trait | heart function measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004311 |
Study accession | GCST000852 |