SNP Detail For rs67180937
1.Mapping Information
Human SNP ID rs67180937
Human chromosome chr1
Human SNP position 222650401
Pig chromosome chr10
Pig SNP position 13553497
2.Annotation Information
PubMed ID26343387
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/26343387
StudyA comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
Disease/TraitCoronary artery disease
Initial sample42,096 European ancestry cases, 361 African American cases, 758 Hispanic American cases, 12,658 South Asian ancestry cases, 1,802 Lebanese ancestry cases, 3,614 East Asian ancestry cases, 99,121 European ancestry controls, 2,778 African American controls,
Replication sampleNA
Region1q41
Chromosome idchr1
Chromosome position222650401
Reported geneMIA3
Mapped geneMIA3
Upstream gene id
Downstream gene id
SNP gene ids375056
Upstream gene distance
Downstream gene distance
SNP risk allelers67180937-G
SNPsrs67180937
Merged
SNP id current67180937
Contextintron_variant
Intergenic0
Allele frequency0.663052
P value0.000000000001
Pvalue mlog12
P value text
Or beta1.08
%95 Ci[1.06- 1.11]
PlatformAffymetrix, Illumina [8600000] (imputed)
CNVN
Mapped traitcoronary artery disease
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000378
Study accessionGCST003116