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

SNP Report

Basic Info
Name rs1539549 dbSNP Ensembl
Location chr13:36451881(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000255448; ENST00000360631; ENST00000379892)
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=0.86, OR=1.14 for whole sample; Binomial P-...... Binomial P-value=0.86, OR=1.14 for whole sample; Binomial P-value=0.6, OR=1.03 for C-subtype More... no significant association no significant association Non-significant
Neale BM, 2008 T:C Uncorrected TDT P-value=1.42E-05 (OR=0.7305); Corrected TDT ...... Uncorrected TDT P-value=1.42E-05 (OR=0.7305); Corrected TDT P-value=2.88E-05 (OR=0.7305) More... One of top 25 results in both uncorrected and corrected TDT ...... One of top 25 results in both uncorrected and corrected TDT test More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1539549 (count: 0) View in gBrowse (chr13:36451881..36451881 )