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

SNP Report

Basic Info
Name rs6770632 dbSNP Ensembl
Location chr3:8793724(Fwd)
Variant Alleles C/A
Ancestral Allele A
Functional Annotation 3_prime_UTR_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000316793)
intron_variant(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 A/C C TDT P-value=0.51, OR=1.21, 95% CI=0.81-1.82. TDT P-value=0.51, OR=1.21, 95% CI=0.81-1.82. TDT analysis did not demonstrate significant association of ...... TDT analysis did not demonstrate significant association of this SNP with ADHD. More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs6770632 (count: 8) View in gBrowse (chr3:8781331..8793724 )
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: 8)