SNP Detail For rs4280164
1.Mapping Information
Human SNP ID rs4280164
Human chromosome chr14
Human SNP position 24302079
Pig chromosome chr7
Pig SNP position 80260243
2.Annotation Information
PubMed ID24571439
JournalGenes Brain Behav
Linkwww.ncbi.nlm.nih.gov/pubmed/24571439
StudyGenome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
Disease/TraitParent of origin effect on language impairment (paternal)
Initial sample153 European ancestry case-parent trios, 54 European ancestry case-mother duos, 12 European ancestry case-father duos, 18 European ancestry cases
Replication sampleNA
Region14q12
Chromosome idchr14
Chromosome position24302079
Reported geneC14orf21, DHRS1, CIDEB, ADCY4, LTB4R
Mapped geneNOP9
Upstream gene id
Downstream gene id
SNP gene ids161424
Upstream gene distance
Downstream gene distance
SNP risk allelers4280164-G
SNPsrs4280164
Merged0
SNP id current4280164
Contextmissense_variant
Intergenic0
Allele frequency0.767
P value0.00000004
Pvalue mlog7.39794000867203
P value text
Or beta3.872
%95 Ci[NR] unit increase
PlatformIllumina [614937]
CNVN
Mapped traitlanguage impairment
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005425
Study accessionGCST002371