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

SNP Report

Basic Info
Name rs16889388 dbSNP Ensembl
Location chr4:13893168(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000503532; ENST00000510907)
nc_transcript_variant(ENST00000503532; ENST00000510907)
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
Yang L, 2013 P-value=0.0000433 P-value=0.0000433 The SNPs associated with P values of 1E-5 or lower The SNPs associated with P values of 1E-5 or lower Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 1)


SNPs in LD with rs16889388 (count: 0) View in gBrowse (chr4:13893168..13893168 )