SNP Detail For rs1886512
1.Mapping Information
Human SNP ID rs1886512
Human chromosome chr13
Human SNP position 73946049
Pig chromosome chr11
Pig SNP position 50758382
2.Annotation Information
PubMed ID21076409
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/21076409
StudyCommon variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
Disease/TraitQRS duration
Initial sample39,717 European ancestry individuals, 690 Orcadian individuals
Replication sample7,170 European ancestry individuals
Region13q22.1
Chromosome idchr13
Chromosome position73946049
Reported geneKLF12
Mapped geneKLF12
Upstream gene id
Downstream gene id
SNP gene ids11278
Upstream gene distance
Downstream gene distance
SNP risk allelers1886512-A
SNPsrs1886512
Merged0
SNP id current1886512
Contextintron_variant
Intergenic0
Allele frequency0.37
P value0.00000001
Pvalue mlog8
P value text
Or beta0.4
%95 Ci[0.26-0.54] ms decrease
PlatformAffymetrix, Illumina [~ 2500000] (imputed)
CNVN
Mapped traitheart function measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004311
Study accessionGCST000872