SNP Detail For rs490592
1.Mapping Information
Human SNP ID rs490592
Human chromosome chr11
Human SNP position 116427650
Pig chromosome chr9
Pig SNP position 48861280
2.Annotation Information
PubMed ID20171287
JournalNeuroimage
Linkwww.ncbi.nlm.nih.gov/pubmed/20171287
StudyVoxelwise genome-wide association study (vGWAS).
Disease/TraitBrain structure
Initial sample740 European ancestry individuals
Replication sampleNA
Region11q23.3
Chromosome idchr11
Chromosome position116427650
Reported geneintergenic
Mapped geneLOC105369513 - LOC101929011
Upstream gene id105369513
Downstream gene id101929011
SNP gene ids
Upstream gene distance346594
Downstream gene distance211772
SNP risk allelers490592-?
SNPsrs490592
Merged0
SNP id current490592
Contextintergenic_variant
Intergenic1
Allele frequency0.21
P value0.000001
Pvalue mlog6
P value text
Or beta
%95 Ci
PlatformIllumina [448293]
CNVN
Mapped traitbrain measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004464
Study accessionGCST000597