SNP Detail For rs4763555
1.Mapping Information
Human SNP ID rs4763555
Human chromosome chr12
Human SNP position 10568857
Pig chromosome chr5
Pig SNP position 64193307
2.Annotation Information
PubMed ID25644384
JournalMol Psychiatry
Linkwww.ncbi.nlm.nih.gov/pubmed/25644384
StudyGenetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53鈥?49).
Disease/TraitCognitive function
Initial sample51,719 European ancestry individuals 1,473 Erasmus Rupchen Family individuals, 327 Korculan individuals, 430 Orcadian individuals
Replication sampleNA
Region12p13.2
Chromosome idchr12
Chromosome position10568857
Reported geneintergenic
Mapped geneLOC105376675, LOC101060038
Upstream gene id
Downstream gene id
SNP gene ids105376675, 101060038
Upstream gene distance
Downstream gene distance
SNP risk allelers4763555-?
SNPsrs4763555
Merged0
SNP id current4763555
Contextintergenic_variant
Intergenic0
Allele frequencyNR
P value0.000009
Pvalue mlog5.04575749056067
P value text
Or beta0.0283
%95 Ci[0.016-0.041] unit increase
PlatformAffymetrix, Illumina [2478500] (imputed)
CNVN
Mapped traitcognition
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003925
Study accessionGCST002774