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

SNP Report

Basic Info
Name rs6657749 dbSNP Ensembl
Location chr1:214576513(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000366956; ENST00000543945)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Lantieri F, 2010 T:C Binomial P-value=0.59, OR=1.03 for whole sample; Binomial P-...... Binomial P-value=0.59, OR=1.03 for whole sample; Binomial P-value=0.76, OR=1.13 for C-subtype More... no significant association no significant association Non-significant
Neale BM, 2008 T:C Corrected TDT P-value=2.99E-05 (OR=0.6643) Corrected TDT P-value=2.99E-05 (OR=0.6643) One of top 25 results in corrected TDT test One of top 25 results in corrected TDT test Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 1)


SNPs in LD with rs6657749 (count: 0) View in gBrowse (chr1:214576513..214576513 )