Linking Disease Associations with Regulatory Information in the Human Genome - Companion website
Marc A. Schaub, Alan P. Boyle, Anshul Kundaje, Serafim Batzoglou, Michael Snyder, Stanford University

Return Home

rs2484873

Associations

Study: Common genetic variation and performance on standardized cognitive tests. [PMID:20125193]
First author: Cirulli ET
Journal: Eur J Hum Genet
Date: 02/03/2010
Phenotype: Cognitive test performance
Study population: Up to 1,086 individuals
Association P-value: 4 x 10-07
Gene: KIAA1217

Lead SNP

rs2484873
Position: chr10:24,634,956 (Open in UCSC Genome Browser)
Distance to nearest TSS: 181,910 bp
GENCODE v7 location: Intron
No regulatory annotation found

Linkage disequilibrium region

Linkage disequilibrium threshold:
 - In all HapMap 2 populations: r2≥0.8 r2≥0.9 r2=1.0 
 - In the HapMap 2 CEU population r2≥0.8 r2≥0.9 r2=1.0 

No SNPs found for this LD threshold.




Credits:
This resource uses data from:
 - The NHGRI GWAS catalog (accessed August 10, 2011)
 - The ENCODE project
 - RegulomeDB
 - The HapMap project

Contact: marc.schaub AT cs.stanford.edu
Last modified: 2011-12-15 01:19:20
SCGPM logo A project of the Center for Genomics and Personalized Medicine at Stanford University. Stanford logo