SNP Detail For rs4658552
1.Mapping Information
Human SNP ID rs4658552
Human chromosome chr1
Human SNP position 243249634
Pig chromosome chr10
Pig SNP position 18531578
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
Region1q43
Chromosome idchr1
Chromosome position243249634
Reported geneSDCCAG8, AKT3
Mapped geneCEP170
Upstream gene id
Downstream gene id
SNP gene ids9859
Upstream gene distance
Downstream gene distance
SNP risk allelers4658552-T
SNPsrs4658552
Merged0
SNP id current4658552
Contextintron_variant
Intergenic0
Allele frequency0.632
P value0.000002
Pvalue mlog5.69897000433601
P value text
Or beta0.021
%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