ADHDgene Database
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Type:
  • Large-scale studies
  • Data Summary
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

SNP Report

Basic Info
Name rs6858066 dbSNP Ensembl
Location Chr4:62754320(Fwd)
Variant Alleles A/G
Ancestral Allele G
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000512091; ENST00000511324; ENST00000514591; ENST00000509896; ENST00000506700; ENST00000507164; ENST00000514157; ENST00000507625; ENST00000508693; ENST00000504896; ENST00000508946; ENST00000514996; ENST00000506746; ENST00000506720; ENST00000545650; ENST00000570545; ENST00000573738; ENST00000577151; ENST00000574812; ENST00000574919; ENST00000573960; ENST00000572342; ENST00000576325; ENST00000576028; ENST00000574839; ENST00000572079; ENST00000576469; ENST00000571630; ENST00000573720)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Ribases M, 2011 allelic P-value=0.025, OR=1.32, genotypic P-value=0.0019, OR...... allelic P-value=0.025, OR=1.32, genotypic P-value=0.0019, OR=1.82 for combined ADHD More... associated with combined ADHD, and remained associated after...... associated with combined ADHD, and remained associated after correcting for multiple testing More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs6858066 (count: 1) View in gBrowse (chr4:62744240..62754320 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.

Literature-origin SNPs (count: 1)

LD-proxies (count: 0)

Copyright: Bioinformatics Lab, Institute of Psychology, Chinese Academy of Sciences Feedback
Last update: Feb 26, 2014