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

SNP Report

Basic Info
Name rs11764590 dbSNP Ensembl
Location chr7:2032803(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000265854; ENST00000399654; ENST00000402746; ENST00000406869; ENST00000438959; ENST00000444373)
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
Schimmelmann, B. G.,2013 Nominal two-sided P-value=0.431 (OR=1.08;95%CI=0.90-1.28) Nominal two-sided P-value=0.431 (OR=1.08;95%CI=0.90-1.28) We found no significant association of childhood ADHD with t...... We found no significant association of childhood ADHD with this locus. More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs11764590 (count: 22) View in gBrowse (chr7:1881527..2110346 )
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: 22)