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

SNP Report

Basic Info
Name rs4913069 dbSNP Ensembl
Location chr5:139545110(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript intron_variant(ENST00000523154)
nc_transcript_variant(ENST00000523154; ENST00000607850)
non_coding_exon_variant(ENST00000607850)
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 A:G Binomial P-value=0.5, OR=0.99 for whole sample; Binomial P-v...... Binomial P-value=0.5, OR=0.99 for whole sample; Binomial P-value=0.69, OR=1.08 for C-subtype More... no significant association no significant association Non-significant
Neale BM, 2008 A:G Uncorrected TDT P-value=6.94E-05 (OR=0.6476) Uncorrected TDT P-value=6.94E-05 (OR=0.6476) One of top 25 results in uncorrected TDT test One of top 25 results in uncorrected TDT test Non-significant

SNP related genes (count: 0)

SNPs in LD with rs4913069 (count: 0) View in gBrowse (chr5:139545110..139545110 )