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

SNP Report

Basic Info
Name rs16965628 dbSNP Ensembl
Location chr17:28555425(Fwd)
Variant Alleles G/C
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000261707; ENST00000394821; ENST00000401766)
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
Landaas ET, 2010 G/C P-value=0.86, OR=0.97 in the Norwegian samples; P-value=0.45...... P-value=0.86, OR=0.97 in the Norwegian samples; P-value=0.45, OR=0.83 in the Norwegian samples; P-value=0.68, OR=1.1 in the Norwegian males More... no significant association no significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs16965628 (count: 23) View in gBrowse (chr17:28555425..28687692 )
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: 23)