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

SNP Report

Basic Info
Name rs3787141 dbSNP Ensembl
Location chr20:61989394(Fwd)
Variant Alleles T/C
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000370263; ENST00000463705; ENST00000467563; ENST00000498043)
nc_transcript_variant(ENST00000463705; ENST00000467563)
NMD_transcript_variant(ENST00000498043)
upstream_gene_variant(ENST00000370257)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Lee J, 2008 T/C P-value=0.166, X2 (1df)=1.921 in all subtypes; P-...... P-value=0.166, X2 (1df)=1.921 in all subtypes; P-value=0.439, X2 (1df)=0.6 in inattentive subtype; P-value=0.046, X2 (1df)=4 in combined subtype; P-value=0.044 in FBAT analysis for hyperactive/impulsive symptoms More... nominally significant evidence of association with the ADHD ...... nominally significant evidence of association with the ADHD combined subtype and with teacher-rated hyperactivity- impulsivity scores More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs3787141 (count: 0) View in gBrowse (chr20:61989394..61989394 )