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

SNP Report

Basic Info
Name rs17729098 dbSNP Ensembl
Location chr20:59077648(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000437035)
nc_transcript_variant(ENST00000437035)
No. of Studies 2 (significant: 0; non-significant: 0; trend: 2)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Neale BM, 2010 (b) T:C GLM P-value=1.68E-06, meta-analysis P-value=0.00000168 GLM P-value=1.68E-06, meta-analysis P-value=0.00000168 One of the top 100 SNPs from imputed IMAGE II dataset One of the top 100 SNPs from imputed IMAGE II dataset Trend
Neale BM, 2010 (a) T:C P-value=1.68E-06 P-value=1.68E-06 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 rs17729098 (count: 0) View in gBrowse (chr20:59077648..59077648 )