SNP Detail For rs4879913
1.Mapping Information
Human SNP ID rs4879913
Human chromosome chr9
Human SNP position 35610915
Pig chromosome chr1
Pig SNP position 264071799
2.Annotation Information
PubMed ID25387704
JournalPsychophysiology
Linkwww.ncbi.nlm.nih.gov/pubmed/25387704
StudyHeritability and molecular-genetic basis of resting EEG activity: A genome-wide association study.
Disease/TraitElectroencephalogram traits
Initial sample2,383 European ancestry adolescents and 1,643 European ancestry adults from 1,613 families
Replication sampleNA
Region9p13.3
Chromosome idchr9
Chromosome position35610915
Reported geneCD72
Mapped geneCD72
Upstream gene id
Downstream gene id
SNP gene ids971
Upstream gene distance
Downstream gene distance
SNP risk allelers4879913-?
SNPsrs4879913
Merged0
SNP id current4879913
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000002
Pvalue mlog5.69897000433601
P value text(Alpha power, Cz)
Or beta0.103
%95 Ci[0.06-0.146] unit decrease
PlatformIllumina [527829]
CNVN
Mapped traitalpha wave measurement, electroencephalogram measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006870, http://www.ebi.ac.uk/efo/EFO_0004357
Study accessionGCST002709