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

SNP Report

Basic Info
Name rs9982805 dbSNP Ensembl
Location chr21:23383609(Fwd)
Variant Alleles C/A
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000416327; ENST00000420255)
nc_transcript_variant(ENST00000416327; ENST00000420255)
No. of Studies 1 (significant: 0; non-significant: 0; trend: 1)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Neale BM, 2010 (a) A:C P-value=2.60E-05 P-value=2.60E-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

SNP related genes (count: 0)

SNPs in LD with rs9982805 (count: 61) View in gBrowse (chr21:23380208..23445840 )
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: 61)