SNP Detail For rs11232369
1.Mapping Information
Human SNP ID rs11232369
Human chromosome chr11
Human SNP position 80851695
Pig chromosome chr9
Pig SNP position 16851772
2.Annotation Information
PubMed ID20125193
JournalEur J Hum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/20125193
StudyCommon genetic variation and performance on standardized cognitive tests.
Disease/TraitCognitive performance
Initial sampleUp to 813 European ancestry individuals, up to 167 East Asian ancestry individuals, up to 7 Hispanic/Latin American individuals, up to 74 South Asian ancestry individuals
Replication sampleNA
Region11q14.1
Chromosome idchr11
Chromosome position80851695
Reported geneAC018897.4
Mapped geneLOC101928964
Upstream gene id
Downstream gene id
SNP gene ids101928964
Upstream gene distance
Downstream gene distance
SNP risk allelers11232369-?
SNPsrs11232369
Merged0
SNP id current11232369
Contextintergenic_variant
Intergenic0
Allele frequencyNR
P value0.000008
Pvalue mlog5.09691001300805
P value text(Digit Span Forward)
Or beta
%95 Ci
PlatformIllumina [up to 563855]
CNVN
Mapped traitneuropsychological test
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003926
Study accessionGCST000579