SNP Detail For rs11897119
1.Mapping Information
Human SNP ID rs11897119
Human chromosome chr2
Human SNP position 66544868
Pig chromosome chr3
Pig SNP position 79180346
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
Region2p14
Chromosome idchr2
Chromosome position66544868
Reported geneMEIS1
Mapped geneMEIS1
Upstream gene id
Downstream gene id
SNP gene ids4211
Upstream gene distance
Downstream gene distance
SNP risk allelers11897119-C
SNPsrs11897119
Merged0
SNP id current11897119
Contextintron_variant
Intergenic0
Allele frequency0.39
P value0.00000000005
Pvalue mlog10.3010299956639
P value text
Or beta1.36
%95 Ci[0.95-1.77] ms increase
PlatformAffymetrix, Illumina [~ 2500000] (imputed)
CNVN
Mapped traitPR interval
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004462
Study accessionGCST000562