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

SNP Report

Basic Info
Name rs9676447 dbSNP Ensembl
Location chr19:49424247(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000424608; ENST00000452087; ENST00000460125)
intron_variant(ENST00000263273; ENST00000405315; ENST00000407032; ENST00000465524; ENST00000469291; ENST00000485798; ENST00000492367)
nc_transcript_variant(ENST00000465524; ENST00000469291; ENST00000485798; ENST00000492367)
upstream_gene_variant(ENST00000416432)
No. of Studies 3 (significant: 0; non-significant: 2; trend: 1)
Source Literature-origin

SNP related studies (count: 3)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Neale BM, 2008 C:T Uncorrected TDT P-value=1.14E-05 (OR=2.078); Corrected TDT P...... Uncorrected TDT P-value=1.14E-05 (OR=2.078); Corrected TDT P-value=1.01E-05 (OR=2.078) More... One of top 25 results in both uncorrected and corrected TDT ...... One of top 25 results in both uncorrected and corrected TDT test More... Non-significant
Neale BM, 2010 (a) T:C P-value=1.25E-05 P-value=1.25E-05 one of top 50 hits from the Genome-Wide Attention-Deficit/Hy...... one of top 50 hits from the Genome-Wide Attention-Deficit/Hyperactivity Disorder (ADHD) meta-analysis More... Trend
Lantieri F, 2010 C:T no P-value no P-value no significant association no significant association Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs9676447 (count: 1) View in gBrowse (chr19:49417658..49424247 )
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: 1)