Human SNP ID | rs2207790 |
---|---|
Human chromosome | chr1 |
Human SNP position | 61432295 |
Pig chromosome | chr6 |
Pig SNP position | 138797620 |
PubMed ID | 23463857 |
---|---|
Journal | Circulation |
Link | www.ncbi.nlm.nih.gov/pubmed/23463857 |
Study | Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk. |
Disease/Trait | Electrocardiographic conduction measures |
Initial sample | 5,272 European ancestry indiviudals |
Replication sample | 40,407 European ancestry individuals |
Region | 1p31.3 |
Chromosome id | chr1 |
Chromosome position | 61432295 |
Reported gene | NFIA |
Mapped gene | NFIA |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4774 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2207790-A |
SNPs | rs2207790 |
Merged | 0 |
SNP id current | 2207790 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.461 |
P value | 0.000000000000000006 |
Pvalue mlog | 17.2218487496163 |
P value text | (QRS duration - CHARGE) |
Or beta | 0.5956 |
%95 Ci | [NR] msec decrease |
Platform | Illumina [528508] |
CNV | N |
Mapped trait | QRS duration |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005055 |
Study accession | GCST001893 |