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 rs6732434 dbSNP Ensembl
Location Chr2:182901257(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000495820; ENST00000475249; ENST00000486067; ENST00000464264; ENST00000409702; ENST00000465612; ENST00000479855; ENST00000409137; ENST00000490645; ENST00000280295; ENST00000452904)
nc_transcript_variant(ENST00000495820; ENST00000475249; ENST00000486067; ENST00000464264; ENST00000465612; ENST00000479855; ENST00000490645)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hinney, A., 2011 A GWAS P-value=4.68E-05, OR=1.41, Replication FBAT P-value=0.0...... GWAS P-value=4.68E-05, OR=1.41, Replication FBAT P-value=0.0042, Combination P-value=2.73E-04 More... This GWAS in a small group of clinically ascertained young G...... This GWAS in a small group of clinically ascertained young German patients with ADHD and population-based controls did not reveal genome-wide significant findings. Replication attempts in further German and international samples did also not lead to a P-value(s) below 5E-08. More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs6732434 (count: 22) View in gBrowse (chr2:182884959..182932398 )
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: 0)

LD-proxies (count: 22)

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