SNP Detail For rs1105881
1.Mapping Information
Human SNP ID rs1105881
Human chromosome chr15
Human SNP position 41780332
Pig chromosome chr1
Pig SNP position 144500726
2.Annotation Information
PubMed ID25201988
JournalProc Natl Acad Sci U S A
Linkwww.ncbi.nlm.nih.gov/pubmed/25201988
StudyCommon genetic variants associated with cognitive performance identified using the proxy-phenotype method.
Disease/TraitEducational attainment
Initial sample106,736 European ancestry individuals
Replication sampleNA
Region15q15.1
Chromosome idchr15
Chromosome position41780332
Reported geneintergenic
Mapped geneMAPKBP1
Upstream gene id
Downstream gene id
SNP gene ids23005
Upstream gene distance
Downstream gene distance
SNP risk allelers1105881-C
SNPsrs1105881
Merged0
SNP id current1105881
Contextintron_variant
Intergenic0
Allele frequency0.643
P value0.000007
Pvalue mlog5.15490195998574
P value text
Or beta0.02
%95 Ci[NR] unit increase
PlatformAffymetrix, Illumina [NR] (imputed)
CNVN
Mapped traitself reported educational attainment
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004784
Study accessionGCST002598