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

SNP Report

Basic Info
Name rs1080750 dbSNP Ensembl
Location chr9:34581525(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000351266; ENST00000378980; ENST00000417345; ENST00000436360; ENST00000438244; ENST00000453642)
nc_transcript_variant(ENST00000436360; ENST00000438244; ENST00000453642)
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, 2008 genotypic P-value=0.12; genotypic P-value=0.14 in dominant m...... genotypic P-value=0.12; genotypic P-value=0.14 in dominant model; genotypic P-value=0.063 in recessive model; allelic P-value=0.048, OR=1.23 (1-1.51) in Children More... provided evidence of association with childhood ADHD provided evidence of association with childhood ADHD Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs1080750 (count: 1) View in gBrowse (chr9:34581525..34669005 )
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)