SNP Detail For rs73267033
1.Mapping Information
Human SNP ID rs73267033
Human chromosome chr12
Human SNP position 7711880
Pig chromosome chr5
Pig SNP position 65687632
2.Annotation Information
PubMed ID26674333
JournalNeurology
Linkwww.ncbi.nlm.nih.gov/pubmed/26674333
StudyGenome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.
Disease/TraitWhite matter hyperintensities in ischemic stroke
Initial sample3,670 European ancestry cases
Replication sampleNA
Region12p13.31
Chromosome idchr12
Chromosome position7711880
Reported geneDPPA3
Mapped geneDPPA3
Upstream gene id
Downstream gene id
SNP gene ids359787
Upstream gene distance
Downstream gene distance
SNP risk allelers73267033-A
SNPsrs73267033
Merged
SNP id current73267033
Contextintron_variant
Intergenic0
Allele frequency0.96
P value0.000002
Pvalue mlog5.69897000433601
P value text
Or beta1.45
%95 Ci[1.25鈥?.69]
PlatformAffymetrix, Illumina [7567914] (imputed)
CNVN
Mapped traitIschemic stroke, white matter hyperintensity measurement
Mapped trait URIhttp://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0005665
Study accessionGCST003245