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

SNP Report

Basic Info
Name rs6561333 dbSNP Ensembl
Location chr13:47420312(Fwd)
Variant Alleles T/C
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000378688; ENST00000542664; ENST00000543956)
No. of Studies 2 (significant: 2; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
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=0.011 for allele analysis in childhood combined ADHD. More... no significance after correcting for multiple comparisons no significance after correcting for multiple comparisons Significant
Oades RD, 2008 P-value=0.012237; FDR P-value=0.12237 for cognitive impulsiv...... P-value=0.012237; FDR P-value=0.12237 for cognitive impulsivity More... attained nominal significance for an association with cognit...... attained nominal significance for an association with cognitive impulsivity More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs6561333 (count: 6) View in gBrowse (chr13:47419204..47421836 )
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)