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

SNP Report

Basic Info
Name rs10761412 dbSNP Ensembl
Location chr9:136519590(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant.
Consequence to Transcript downstream_gene_variant(ENST00000425189)
intron_variant(ENST00000393056)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hawi, Z., 2012 T:C C P-value=0.4268, X2=0.63, OR=1.11, 95% CI=0.86-1.4...... P-value=0.4268, X2=0.63, OR=1.11, 95% CI=0.86-1.43 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs10761412 (count: 0) View in gBrowse (chr9:136519590..136519590 )