Human SNP ID | rs10476160 |
---|---|
Human chromosome | chr5 |
Human SNP position | 175547573 |
Pig chromosome | chr2 |
Pig SNP position | 83633287 |
PubMed ID | 23509962 |
---|---|
Journal | BMC Med Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23509962 |
Study | A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. |
Disease/Trait | Venous thromboembolism (SNP x SNP interaction) |
Initial sample | 411 European ancestry cases, 1,228 European ancestry controls |
Replication sample | 1,542 European ancestry cases, 1,110 European ancestry controls |
Region | 5q35.2 x 8p23.2 |
Chromosome id | chr5 x 8 |
Chromosome position | 175547573 x 5750141 |
Reported gene | NR x NR |
Mapped gene | SFXN1 - HRH2 x LOC105377794 - LOC105377795 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10476160-? x rs1707420-? |
SNPs | rs10476160 x rs1707420 |
Merged | 0 |
SNP id current | |
Context | intergenic_variant x intergenic_variant |
Intergenic | |
Allele frequency | |
P value | 0.000000009 |
Pvalue mlog | 8.04575749056067 |
P value text | |
Or beta | 1.6129 |
%95 Ci | [NR] |
Platform | Illumina [291872] |
CNV | N |
Mapped trait | venous thromboembolism |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004286 |
Study accession | GCST001913 |