SNP Detail For rs10166311
1.Mapping Information
Human SNP ID rs10166311
Human chromosome chr2
Human SNP position 162011103
Pig chromosome chr15
Pig SNP position 76171635
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
Region2q24.2
Chromosome idchr2
Chromosome position162011103
Reported geneintergenic
Mapped geneDPP4
Upstream gene id
Downstream gene id
SNP gene ids1803
Upstream gene distance
Downstream gene distance
SNP risk allelers10166311-A
SNPsrs10166311
Merged0
SNP id current10166311
Contextintron_variant
Intergenic0
Allele frequency0.326
P value0.000001
Pvalue mlog6
P value text
Or beta0.023
%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