Human SNP ID | rs10504130 |
---|---|
Human chromosome | chr8 |
Human SNP position | 51844533 |
Pig chromosome | chr4 |
Pig SNP position | 85368910 |
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 | 8q11.23 x 18p11.22 |
Chromosome id | chr8 x 18 |
Chromosome position | 51844533 x 10447044 |
Reported gene | NR x NR |
Mapped gene | PCMTD1 x LOC105371988 - APCDD1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10504130-A x rs2847351-G |
SNPs | rs10504130 x rs2847351 |
Merged | 0 |
SNP id current | |
Context | intron_variant x intergenic_variant |
Intergenic | |
Allele frequency | |
P value | 0.000000004 |
Pvalue mlog | 8.39794000867203 |
P value text | |
Or beta | 1.88 |
%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 |