SNP Detail For rs7306642
1.Mapping Information
Human SNP ID rs7306642
Human chromosome chr12
Human SNP position 103745256
Pig chromosome chr5
Pig SNP position 84247482
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
Region12q23.3
Chromosome idchr12
Chromosome position103745256
Reported geneSTAB2
Mapped geneSTAB2
Upstream gene id
Downstream gene id
SNP gene ids55576
Upstream gene distance
Downstream gene distance
SNP risk allelers7306642-A
SNPsrs7306642
Merged0
SNP id current7306642
Contextmissense_variant
Intergenic0
Allele frequency0.07
P value0.000003
Pvalue mlog5.52287874528033
P value text(FVIII Activity)
Or beta0.3
%95 Ci[0.18-0.42] IU/dL increase
PlatformIllumina [442728]
CNVN
Mapped traitfactor VIII measurement, coagulation factor measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004630, http://www.ebi.ac.uk/efo/EFO_0004634
Study accessionGCST001188