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

SNP Report

Basic Info
Name rs7322347 dbSNP Ensembl
Location chr13:47410103(Fwd)
Variant Alleles T/A
Ancestral Allele A
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000378688; ENST00000542664; ENST00000543956)
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=0.03 for genotype analysis...... Case-control test: lowest P-value=0.03 for genotype analysis, P-value=0.3 for allele analysis in all adult ADHD; lowest P-value=0.014 for genotype analysis, P-value=0.13 for allele analysis in adult combined ADHD. | lowest P-value=0.018 for genotype analysis, P-value=0.0085 for allele analysis in all childhood ADHD; lowest P-value=0.0053 for genotype analysis, P-value=0.0015 for allele analysis in childhood combined ADHD. More... Still significant associated with childhood combined ADHD af...... Still significant associated with childhood combined ADHD after correcting for multiple comparisons More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs7322347 (count: 6) View in gBrowse (chr13:47403360..47415001 )
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: 6)