SNP Detail For rs6454764
1.Mapping Information
Human SNP ID rs6454764
Human chromosome chr6
Human SNP position 89601247
Pig chromosome chr1
Pig SNP position 64517698
2.Annotation Information
PubMed ID21810271
JournalBMC Med Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/21810271
StudyCombined analysis of three genome-wide association studies on vWF and FVIII plasma levels.
Disease/TraitvWF and FVIII levels
Initial sample1,624 European ancestry individuals
Replication sampleNA
Region6q15
Chromosome idchr6
Chromosome position89601247
Reported geneANKRD6
Mapped geneANKRD6
Upstream gene id
Downstream gene id
SNP gene ids22881
Upstream gene distance
Downstream gene distance
SNP risk allelers6454764-T
SNPsrs6454764
Merged0
SNP id current6454764
Contextintron_variant
Intergenic0
Allele frequency0.06
P value0.000005
Pvalue mlog5.30102999566398
P value text(vWF levels)
Or beta0.31
%95 Ci[0.17-0.45] IU/dL increase
PlatformIllumina [442728]
CNVN
Mapped traitvon Willebrand factor measurement, coagulation factor measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004629, http://www.ebi.ac.uk/efo/EFO_0004634
Study accessionGCST001188