Human SNP ID | rs9390459 |
---|---|
Human chromosome | chr6 |
Human SNP position | 147359223 |
Pig chromosome | chr1 |
Pig SNP position | 20564801 |
PubMed ID | 20231535 |
---|---|
Journal | Circulation |
Link | www.ncbi.nlm.nih.gov/pubmed/20231535 |
Study | Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. |
Disease/Trait | vWF levels |
Initial sample | 17,596 European ancestry individuals |
Replication sample | Up to 7,604 European ancestry individuals |
Region | 6q24.3 |
Chromosome id | chr6 |
Chromosome position | 147359223 |
Reported gene | STXBP5 |
Mapped gene | STXBP5 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 134957 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs9390459-? |
SNPs | rs9390459 |
Merged | 0 |
SNP id current | 9390459 |
Context | synonymous_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 1E-22 |
Pvalue mlog | 22 |
P value text | |
Or beta | 4.8 |
%95 Ci | [2.1-7.5] unit decrease |
Platform | Affymetrix, Illumina [2742821] (imputed) |
CNV | N |
Mapped trait | von Willebrand factor measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004629 |
Study accession | GCST000627 |