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

SNP Report

Basic Info
Name rs16838844 dbSNP Ensembl
Location chr4:6440620(Fwd)
Variant Alleles T/G
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000314348; ENST00000382599; ENST00000506140; ENST00000507028; ENST00000507294)
nc_transcript_variant(ENST00000314348; ENST00000507028)
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
Jacob, C., 2012 G P-value=0.1271, OR=1.1595% CI=(0.96-1.37) in the adult case-...... P-value=0.1271, OR=1.1595% CI=(0.96-1.37) in the adult case-control sample; FBAT P-value=0.0469 in the families with ADHD children More... It reached nominal significance, however not surviving corre...... It reached nominal significance, however not surviving correction for multiple testing in the children sample; Furthermore, we observed a nominal p value of 0.032 for SNP rs16838844 in the adult sample when only combined-type cases were considered. More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs16838844 (count: 6) View in gBrowse (chr4:6425624..6443045 )
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)