Human SNP ID | rs12344583 |
---|---|
Human chromosome | chr9 |
Human SNP position | 133858398 |
Pig chromosome | chr1 |
Pig SNP position | 307354111 |
PubMed ID | 21810271 |
---|---|
Journal | BMC Med Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/21810271 |
Study | Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. |
Disease/Trait | vWF and FVIII levels |
Initial sample | 1,624 European ancestry individuals |
Replication sample | NA |
Region | 9q34.2 |
Chromosome id | chr9 |
Chromosome position | 133858398 |
Reported gene | VAV2 |
Mapped gene | VAV2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 7410 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs12344583-G |
SNPs | rs12344583 |
Merged | 0 |
SNP id current | 12344583 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.2 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (FVIII activity) |
Or beta | 0.2 |
%95 Ci | [0.12-0.28] IU/dL increase |
Platform | Illumina [442728] |
CNV | N |
Mapped trait | factor VIII measurement, coagulation factor measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004630, http://www.ebi.ac.uk/efo/EFO_0004634 |
Study accession | GCST001188 |