SNP Detail For rs1763510
1.Mapping Information
Human SNP ID rs1763510
Human chromosome chr6
Human SNP position 134236069
Pig chromosome chr1
Pig SNP position 33207205
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
Region1p22.3 x 6q23.2
Chromosome idchr1 x 6
Chromosome position85066028 x 134236069
Reported geneNR x NR
Mapped geneWDR63 x SGK1
Upstream gene id
Downstream gene id
SNP gene ids
Upstream gene distance
Downstream gene distance
SNP risk allelers6695223-C x rs1763510-T
SNPsrs6695223 x rs1763510
Merged0
SNP id current
Contextintron_variant x intron_variant
Intergenic
Allele frequency
P value0.000000005
Pvalue mlog8.30102999566398
P value text
Or beta1.86
%95 Ci[NR]
PlatformIllumina [291872]
CNVN
Mapped traitvenous thromboembolism
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004286
Study accessionGCST001913