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

SNP Report

Basic Info
Name rs3763965 dbSNP Ensembl
Location chr11:27528987(Fwd)
Variant Alleles A/T
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000499008; ENST00000499568; ENST00000500662; ENST00000501176; ENST00000502161; ENST00000530686; ENST00000532965)
nc_transcript_variant(ENST00000499008; ENST00000499568; ENST00000500662; ENST00000501176; ENST00000502161; ENST00000530686; ENST00000532965)
upstream_gene_variant(ENST00000278193; ENST00000524596)
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
Lanktree M, 2008 A:T X2=0.67, P-value=0.41 in the family-based sample;...... X2=0.67, P-value=0.41 in the family-based sample; X2=0.04, P-value=0.85, OR=1.04 in the case-control sample; X2=0.2, P-value=0.65, OR=1.07 in the combined samples More... no significant differences were observed in all samples no significant differences were observed in all samples Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs3763965 (count: 20) View in gBrowse (chr11:27461779..27628826 )
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: 20)