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

SNP Report

Basic Info
Name rs6592961 dbSNP Ensembl
Location chr7:50572890(Fwd)
Variant Alleles G/A
Ancestral Allele A
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000357936; ENST00000380984; ENST00000426377; ENST00000430300; ENST00000431062; ENST00000444124; ENST00000444733)
NMD_transcript_variant(ENST00000444733)
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=0.00067 for genotype analy...... Case-control test: lowest P-value=0.00067 for genotype analysis, P-value=0.0029 for allele analysis in all adult ADHD; lowest P-value=0.00059 for genotype analysis, P-value=0.0018 for allele analysis in adult combined ADHD. | lowest P-value=1.90E-06 for genotype analysis, P-value=2.03E-05 for allele analysis in all childhood ADHD; lowest P-value=7.20E-05 for genotype analysis, P-value=0.00053 for allele analysis in childhood combined ADHD; lowest P-value=0.00061 for genotype analysis, P-value=0.0014 for allele analysis in childhood inattentive ADHD. More... Still significant associated with all ADHD and combined ADHD...... Still significant associated with all ADHD and combined ADHD in adult and childhood groups after correcting for multiple comparisons, as well as in childhood inattentive ADHD group More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs6592961 (count: 18) View in gBrowse (chr7:50544314..50615840 )
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: 18)