SNP Detail For rs4944092
1.Mapping Information
Human SNP ID rs4944092
Human chromosome chr11
Human SNP position 76198575
Pig chromosome chr9
Pig SNP position 11601412
2.Annotation Information
PubMed ID20062060
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/20062060
StudyGenome-wide association study of PR interval.
Disease/TraitPR interval
Initial sample28,517 European ancestry individuals
Replication sampleNA
Region11q13.5
Chromosome idchr11
Chromosome position76198575
Reported geneWNT11
Mapped geneWNT11
Upstream gene id
Downstream gene id
SNP gene ids7481
Upstream gene distance
Downstream gene distance
SNP risk allelers4944092-G
SNPsrs4944092
Merged0
SNP id current4944092
Contextintron_variant
Intergenic0
Allele frequency0.32
P value0.00000003
Pvalue mlog7.52287874528033
P value text
Or beta1.19
%95 Ci[0.77-1.61] ms decrease
PlatformAffymetrix, Illumina [~ 2500000] (imputed)
CNVN
Mapped traitPR interval
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004462
Study accessionGCST000562