SNP Detail For rs4937126
1.Mapping Information
Human SNP ID rs4937126
Human chromosome chr11
Human SNP position 126412002
Pig chromosome chr9
Pig SNP position 59321174
2.Annotation Information
PubMed ID21378990
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/21378990
StudyLarge-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
Disease/TraitCoronary heart disease
Initial sample22,233 European ancestry cases, 64,762 European ancestry controls
Replication sample56,682 European ancestry cases and controls
Region11q24.2
Chromosome idchr11
Chromosome position126412002
Reported geneintergenic
Mapped geneST3GAL4
Upstream gene id
Downstream gene id
SNP gene ids6484
Upstream gene distance
Downstream gene distance
SNP risk allelers4937126-G
SNPsrs4937126
Merged0
SNP id current4937126
Contextintron_variant
Intergenic0
Allele frequency0.69
P value0.000005
Pvalue mlog5.30102999566398
P value text
Or beta1.06
%95 Ci[1.04-1.09]
PlatformAffymetrix, Illumina [~ 2300000] (imputed)
CNVN
Mapped traitcoronary heart disease
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001645
Study accessionGCST000998