ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

SNP Report

Basic Info
Name rs4732641 dbSNP Ensembl
Location chr8:26617904(Fwd)
Variant Alleles A/C
Ancestral Allele A
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000380581; ENST00000380582; ENST00000380586; ENST00000380587; ENST00000519096; ENST00000519229; ENST00000521711)
NMD_transcript_variant(ENST00000519096; ENST00000521711)
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
Hawi, Z., 2012 A:C C P-value=0.3195, X2=0.99, OR=1.14, 95% CI=0.88-1.4...... P-value=0.3195, X2=0.99, OR=1.14, 95% CI=0.88-1.48 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 0)


SNPs in LD with rs4732641 (count: 6) View in gBrowse (chr8:26613408..26648746 )
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: 6)