SNP Detail For rs2970992
1.Mapping Information
Human SNP ID rs2970992
Human chromosome chr2
Human SNP position 100705847
Pig chromosome chr3
Pig SNP position 56143193
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
Region2q11.2
Chromosome idchr2
Chromosome position100705847
Reported geneNPAS2, NMS
Mapped geneNANOGNBP1 - LOC105373508
Upstream gene id100859926
Downstream gene id105373508
SNP gene ids
Upstream gene distance44903
Downstream gene distance34100
SNP risk allelers2970992-A
SNPsrs2970992
Merged0
SNP id current2970992
Contextintergenic_variant
Intergenic1
Allele frequency0.493
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