SNP Detail For rs4276643
1.Mapping Information
Human SNP ID rs4276643
Human chromosome chr8
Human SNP position 27946082
Pig chromosome chr14
Pig SNP position 12925863
2.Annotation Information
PubMed ID26486471
JournalEur J Hum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/26486471
StudyGenome-wide association studies identify genetic loci for low von Willebrand factor levels.
Disease/TraitLow vWF levels
Initial sampleup to 1,635 European ancestry individuals with low vWF levels, up to 33,286 European ancestry individuals with normal vWF levels
Replication sampleNA
Region8p21.1
Chromosome idchr8
Chromosome position27946082
Reported geneSCARA5
Mapped geneSCARA5
Upstream gene id
Downstream gene id
SNP gene ids286133
Upstream gene distance
Downstream gene distance
SNP risk allelers4276643-?
SNPsrs4276643
Merged0
SNP id current4276643
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.0000003
Pvalue mlog6.52287874528033
P value text
Or beta
%95 Ci
PlatformAffymetrix, Illumina [~ 2600000] (imputed)
CNVN
Mapped traitvon Willebrand factor measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004629
Study accessionGCST003210