SNP Detail For rs11191193
1.Mapping Information
Human SNP ID rs11191193
Human chromosome chr10
Human SNP position 102042651
Pig chromosome chr14
Pig SNP position 122914142
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
Region10q24.32
Chromosome idchr10
Chromosome position102042651
Reported geneintergenic
Mapped geneC10orf76
Upstream gene id
Downstream gene id
SNP gene ids79591
Upstream gene distance
Downstream gene distance
SNP risk allelers11191193-A
SNPsrs11191193
Merged0
SNP id current11191193
Contextintron_variant
Intergenic0
Allele frequency0.653
P value0.0000006
Pvalue mlog6.22184874961635
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