Human SNP ID | rs11897119 |
---|---|
Human chromosome | chr2 |
Human SNP position | 66544868 |
Pig chromosome | chr3 |
Pig SNP position | 79180346 |
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 | 2p14 |
Chromosome id | chr2 |
Chromosome position | 66544868 |
Reported gene | MEIS1 |
Mapped gene | MEIS1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4211 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11897119-C |
SNPs | rs11897119 |
Merged | 0 |
SNP id current | 11897119 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.39 |
P value | 0.00000000005 |
Pvalue mlog | 10.3010299956639 |
P value text | |
Or beta | 1.36 |
%95 Ci | [0.95-1.77] ms increase |
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 |