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

SNP Report

Basic Info
Name rs10835188 dbSNP Ensembl
Location chr11:27523186(Fwd)
Variant Alleles G/T
Ancestral Allele G
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000278193; ENST00000524596)
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
Lanktree M, 2008 A:C X2=6.42, P-value=0.011 in the family-based sample...... X2=6.42, P-value=0.011 in the family-based sample; X2=1.85, P-value=0.17, OR=1.36 in the case-control sample; X2=7.26, P-value=0.0071, OR=1.61 in the combined samples More... C allele was significantly over-transmitted to Adult ADHD pr...... C allele was significantly over-transmitted to Adult ADHD probands in the family-based sample, and showed association in the combined samples More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs10835188 (count: 25) View in gBrowse (chr11:27505954..27627296 )
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: 25)