SNP Detail For rs247929
1.Mapping Information
Human SNP ID rs247929
Human chromosome chr12
Human SNP position 45901125
Pig chromosome chr5
Pig SNP position 79720310
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
Region12q12
Chromosome idchr12
Chromosome position45901125
Reported geneintergenic
Mapped geneARID2
Upstream gene id
Downstream gene id
SNP gene ids196528
Upstream gene distance
Downstream gene distance
SNP risk allelers247929-C
SNPsrs247929
Merged0
SNP id current247929
Contextintron_variant
Intergenic0
Allele frequency0.513
P value0.000008
Pvalue mlog5.09691001300805
P value text
Or beta0.02
%95 Ci[NR] unit decrease
PlatformAffymetrix, Illumina [NR] (imputed)
CNVN
Mapped traitself reported educational attainment
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004784
Study accessionGCST002598