Human SNP ID | rs6454764 |
---|---|
Human chromosome | chr6 |
Human SNP position | 89601247 |
Pig chromosome | chr1 |
Pig SNP position | 64517698 |
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 | 6q15 |
Chromosome id | chr6 |
Chromosome position | 89601247 |
Reported gene | ANKRD6 |
Mapped gene | ANKRD6 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 22881 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6454764-T |
SNPs | rs6454764 |
Merged | 0 |
SNP id current | 6454764 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.06 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | (vWF levels) |
Or beta | 0.31 |
%95 Ci | [0.17-0.45] IU/dL increase |
Platform | Illumina [442728] |
CNV | N |
Mapped trait | von Willebrand factor measurement, coagulation factor measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004629, http://www.ebi.ac.uk/efo/EFO_0004634 |
Study accession | GCST001188 |