Human SNP ID | rs4715555 |
---|---|
Human chromosome | chr6 |
Human SNP position | 55583812 |
Pig chromosome | chr7 |
Pig SNP position | 30062705 |
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 | 1p31.3 x 6p12.1 |
Chromosome id | chr1 x 6 |
Chromosome position | 65230247 x 55583812 |
Reported gene | NR x NR |
Mapped gene | AK4 x HMGCLL1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1336472-A x rs4715555-G |
SNPs | rs1336472 x rs4715555 |
Merged | 0 |
SNP id current | |
Context | 3_prime_UTR_variant x upstream_gene_variant |
Intergenic | |
Allele frequency | |
P value | 0.0000000004 |
Pvalue mlog | 9.39794000867203 |
P value text | |
Or beta | 1.54 |
%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 |