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

SNP Report

Basic Info
Name rs237895 dbSNP Ensembl
Location chr3:8807423(Fwd)
Variant Alleles T/C
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000431493; ENST00000449615; ENST00000474615)
intron_variant(ENST00000316793; ENST00000472766)
nc_transcript_variant(ENST00000472766)
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
Park J, 2010 C/T C TDT P-value=0.64, OR=1.13, 95% CI=0.78-1.64. TDT P-value=0.64, OR=1.13, 95% CI=0.78-1.64. TDT analysis did not demonstrate significant association of ...... TDT analysis did not demonstrate significant association of this SNP with ADHD. But an association with social cognitive impairments in a subset of the ADHD probands (N=112) was found for this SNP (F=3.09, P-value=0.05). More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs237895 (count: 1) View in gBrowse (chr3:8807423..8808285 )
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)