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

SNP Report

Basic Info
Name rs7984966 dbSNP Ensembl
Location chr13:47429446(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000452352)
intron_variant(ENST00000378688; ENST00000430913; ENST00000455126; ENST00000542664; ENST00000543956)
nc_transcript_variant(ENST00000430913; ENST00000455126)
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
Ribases M, 2009(b) Case-control test: lowest P-value=0.05 for genotype analysis...... Case-control test: lowest P-value=0.05 for genotype analysis, P-value=0.024 for allele analysis in all adult ADHD; lowest P-value=0.0012 for genotype analysis, P-value=0.0019 for allele analysis in adult combined ADHD. | lowest P-value=0.033 for genotype analysis, P-value=0.039 for allele analysis in all childhood ADHD; lowest P-value=0.0097 for genotype analysis, P-value=0.011 for allele analysis in childhood combined ADHD. More... Still significant associated with adult combined ADHD after ...... Still significant associated with adult combined ADHD after correcting for multiple comparisons More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs7984966 (count: 0) View in gBrowse (chr13:47429446..47429446 )