SNP Detail For rs884483
1.Mapping Information
Human SNP ID rs884483
Human chromosome chr15
Human SNP position 70109970
Pig chromosome chr1
Pig SNP position 185954245
2.Annotation Information
PubMed ID23509962
JournalBMC Med Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23509962
StudyA genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
Disease/TraitVenous thromboembolism (SNP x SNP interaction)
Initial sample411 European ancestry cases, 1,228 European ancestry controls
Replication sample1,542 European ancestry cases, 1,110 European ancestry controls
Region12q15 x 15q23
Chromosome idchr12 x 15
Chromosome position69377293 x 70109970
Reported geneNR x NR
Mapped geneYEATS4 x TLE3 - LOC105370878
Upstream gene id
Downstream gene id
SNP gene ids
Upstream gene distance
Downstream gene distance
SNP risk allelers315122-G x rs884483-C
SNPsrs315122 x rs884483
Merged0
SNP id current
Contextintron_variant x intergenic_variant
Intergenic
Allele frequency
P value0.000000001
Pvalue mlog9
P value text
Or beta2.05
%95 Ci[NR]
PlatformIllumina [291872]
CNVN
Mapped traitvenous thromboembolism
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004286
Study accessionGCST001913