Human SNP ID | rs13375391 |
---|---|
Human chromosome | chr1 |
Human SNP position | 185825751 |
Pig chromosome | JH118958-1 |
Pig SNP position | 192557 |
PubMed ID | 23534349 |
---|---|
Journal | Ann Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23534349 |
Study | Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans. |
Disease/Trait | QRS duration |
Initial sample | 455 African American individuals |
Replication sample | NA |
Region | 1q31.1 |
Chromosome id | chr1 |
Chromosome position | 185825751 |
Reported gene | HMCN1 |
Mapped gene | HMCN1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 83872 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs13375391-A |
SNPs | rs13375391 |
Merged | 0 |
SNP id current | 13375391 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000009 |
Pvalue mlog | 5.04575749056067 |
P value text | |
Or beta | 5.82 |
%95 Ci | [NR] ms increase |
Platform | Illumina [> 930000] |
CNV | N |
Mapped trait | QRS duration |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005055 |
Study accession | GCST001920 |