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

SNP Report

Basic Info
Name rs2327269 dbSNP Ensembl
Location chr20:10303128(Fwd)
Variant Alleles T/C
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000421143; ENST00000453544)
nc_transcript_variant(ENST00000421143; ENST00000453544)
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
Kim JW, 2007 T/C C Single marker analysis FBAT P-value=0.013; Exploratory analy...... Single marker analysis FBAT P-value=0.013; Exploratory analyses FBAT P-value=0.248 for co-morbid CD, P-value=0.013 for co-morbid MDD, P-value=0.127 for co-morbid BD More... Single marker and exploratory analysis showed evidence of si...... Single marker and exploratory analysis showed evidence of significant association with ADHD and co-morbid MDD More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 1)


SNPs in LD with rs2327269 (count: 0) View in gBrowse (chr20:10303128..10303128 )