SNP Detail For rs7788657
1.Mapping Information
Human SNP ID rs7788657
Human chromosome chr7
Human SNP position 13882516
Pig chromosome chr9
Pig SNP position 91492488
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
Region7p21.2
Chromosome idchr7
Chromosome position13882516
Reported geneintergenic
Mapped geneRPL26P21 - ETV1
Upstream gene id646161
Downstream gene id2115
SNP gene ids
Upstream gene distance9960
Downstream gene distance8713
SNP risk allelers7788657-T
SNPsrs7788657
Merged0
SNP id current7788657
Contextintergenic_variant
Intergenic1
Allele frequency0.436
P value0.0000009
Pvalue mlog6.04575749056067
P value text
Or beta0.056
%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