SNP Detail For rs1333042
1.Mapping Information
Human SNP ID rs1333042
Human chromosome chr9
Human SNP position 22103814
Pig chromosome chr1
Pig SNP position 223820513
2.Annotation Information
PubMed ID23364394
JournalJ Hum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23364394
StudyA genome-wide association study of a coronary artery disease risk variant.
Disease/TraitCoronary heart disease
Initial sample2,123 Korean ancestry cases, 3,591 Korean ancestry controls
Replication sample3,052 Japanese ancestry cases, 4,976 Japanese ancestry controls
Region9p21.3
Chromosome idchr9
Chromosome position22103814
Reported geneCDKN2A/2B
Mapped geneCDKN2B-AS1
Upstream gene id
Downstream gene id
SNP gene ids100048912
Upstream gene distance
Downstream gene distance
SNP risk allelers1333042-?
SNPsrs1333042
Merged0
SNP id current1333042
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000000001
Pvalue mlog9
P value text
Or beta1.3
%95 Ci[1.19-1.41]
PlatformAffymetrix [521786]
CNVN
Mapped traitcoronary heart disease
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001645
Study accessionGCST001845