SNP Detail For rs4668356
1.Mapping Information
Human SNP ID rs4668356
Human chromosome chr2
Human SNP position 170965956
Pig chromosome chr15
Pig SNP position 86512722
2.Annotation Information
PubMed ID19734545
JournalHum Mol Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/19734545
StudyA genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
Disease/TraitCognitive performance
Initial sampleUp to 1,295 individuals
Replication sampleNA
Region2q31.1
Chromosome idchr2
Chromosome position170965956
Reported geneGORASP2
Mapped geneGORASP2
Upstream gene id
Downstream gene id
SNP gene ids26003
Upstream gene distance
Downstream gene distance
SNP risk allelers4668356-?
SNPsrs4668356
Merged0
SNP id current4668356
Contextsynonymous_variant
Intergenic0
Allele frequency0.06041
P value0.000001
Pvalue mlog6
P value text(PAL8)
Or beta
%95 Ci
PlatformIllumina [475971]
CNVN
Mapped traitneuropsychological test
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003926
Study accessionGCST000477