Human SNP ID | rs7722600 |
---|---|
Human chromosome | chr5 |
Human SNP position | 137859073 |
Pig chromosome | chr2 |
Pig SNP position | 145611775 |
PubMed ID | 23583979 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23583979 |
Study | Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. |
Disease/Trait | Heart rate |
Initial sample | 85,787 European ancestry individuals, 6,568 Indian Asian ancestry indiviudals |
Replication sample | 88,823 European ancestry individuals |
Region | 5q31.2 |
Chromosome id | chr5 |
Chromosome position | 137859073 |
Reported gene | MYOT |
Mapped gene | LOC101928005 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101928005 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7722600-A |
SNPs | rs7722600 |
Merged | 0 |
SNP id current | 7722600 |
Context | non_coding_transcript_exon_variant |
Intergenic | 0 |
Allele frequency | 0.815 |
P value | 0.0000003 |
Pvalue mlog | 6.52287874528033 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix, Illumina [2516789] (imputed) |
CNV | N |
Mapped trait | heart rate |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004326 |
Study accession | GCST001969 |