SNP Detail For rs147852159
1.Mapping Information
Human SNP ID rs147852159
Human chromosome chr8
Human SNP position 144945778
Pig chromosome chr4
Pig SNP position 135663
2.Annotation Information
PubMed ID25663218
JournalCirc Cardiovasc Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25663218
StudyMultiethnic genome-wide association study of cerebral white matter hyperintensities on MRI.
Disease/TraitWhite matter hyperintensity burden
Initial sample17,936 European ancestry individuals, 1,943 African American ancestry individuals, 795 Hispanic individuals, 204 Chinese ancestry individuals, 201 Malay ancestry individuals
Replication sampleNA
Region8q24.3
Chromosome idchr8
Chromosome position144945778
Reported geneZNF16
Mapped geneZNF16
Upstream gene id
Downstream gene id
SNP gene ids7564
Upstream gene distance
Downstream gene distance
SNP risk allelers147852159-G
SNPsrs147852159
Merged
SNP id current147852159
Contextnon_coding_transcript_exon_variant
Intergenic0
Allele frequency0.03
P value0.0000003
Pvalue mlog6.52287874528033
P value text(AA)
Or beta
%95 Ci
PlatformAffymetrix, Illumina [14227402] (imputed)
CNVN
Mapped traitwhite matter hyperintensity measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005665
Study accessionGCST003013