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

SNP Report

Basic Info
Name rs6269 dbSNP Ensembl
Location chr22:19949952(Fwd)
Variant Alleles A/G
Ancestral Allele G
Functional Annotation 5_prime_UTR_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript 5_prime_UTR_variant(ENST00000403710)
intron_variant(ENST00000207636; ENST00000361682; ENST00000403184; ENST00000406520; ENST00000407537; ENST00000412786; ENST00000467943)
upstream_gene_variant(ENST00000428707; ENST00000449653; ENST00000493893; ENST00000585066)
No. of Studies 2 (significant: 1; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Nyman ES, 2007 No available information. No available information. No evidence of association was seen. No evidence of association was seen. Non-significant
Halleland H, 2009 G/A Single marker test: P-value=0.62 (OR=1.05 [0.86-1.29]); Quan...... Single marker test: P-value=0.62 (OR=1.05 [0.86-1.29]); Quantitative linear regression analysis: P-value=0.007 (beta=0.83) for hyperactivity subscale; P-value=0.61 (beta=-0.15) for inattention subscale; P-value=0.21 (beta=0.68) for ASRS total More... no association with ADHD, but strongest association with hyp...... no association with ADHD, but strongest association with hyperactivity/impulsivity. More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)

SNPs in LD with rs6269 (count: 0) View in gBrowse (chr22:19949952..19949952 )