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

SNP Report

Basic Info
Name rs12861247 dbSNP Ensembl
Location chrX:7174199(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000217961)
No. of Studies 3 (significant: 2; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 3)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Stergiakouli E, 2011 G/A P-value=0.762, OR=1.08 in the total sample of case-control a...... P-value=0.762, OR=1.08 in the total sample of case-control analysis; P-value=0.888, OR=0.96 in males only More... there was no significant difference between cases and contro...... there was no significant difference between cases and controls More... Non-significant
Brookes KJ, 2010 TDT P-value=0.01, OR=1.88 TDT P-value=0.01, OR=1.88 was previously genotyped and still significant in this large...... was previously genotyped and still significant in this larger sample but cannot survive stringent correction for multiple testing; also associated with reduced STS mRNA expression in normal human post-mortem frontal cortex brain tissue compared to the non-risk allele (P-value=0.01) More... Significant
Brookes KJ, 2008(b) TDT P-value=0.0055, OR=2.05; Bonferroni correction P-value=0...... TDT P-value=0.0055, OR=2.05; Bonferroni correction P-value=0.0385; P-value=0.015 for males only More... remains significant after correction; significantly associat...... remains significant after correction; significantly associated with male probands More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs12861247 (count: 0) View in gBrowse (chrX:7174199..7174199 )