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

SNP Report

Basic Info
Name rs265977 dbSNP Ensembl
Location chr5:174863257(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation downstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000393752)
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., 2012 genotypic P-value=2.0E-04, genotype 11 vs 12+22: P-value=0.0...... genotypic P-value=2.0E-04, genotype 11 vs 12+22: P-value=0.002, OR (95% CI)=1.72 (1.22-2.44); genotype 11 +12 vs. 22: P-value=7E-04, OR (95% CI)=7.69(1.75-33.3); allelic P-value=2.1E-04, OR (95% CI)=1.77(1.30-2.40) More... Four SNPs in DRD1 displayed nominal associations with ADHD i...... Four SNPs in DRD1 displayed nominal associations with ADHD in the childhood dataset. After applying the Bonferroni correction, only rs265977 in DRD1 remained associated with ADHD in children More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs265977 (count: 1) View in gBrowse (chr5:174862420..174863257 )
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: 1)