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

SNP Report

Basic Info
Name rs930072 dbSNP Ensembl
Location chr5:36666071(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000510740)
intron_variant(ENST00000265113; ENST00000381918; ENST00000509272; ENST00000514563)
nc_transcript_variant(ENST00000509272; ENST00000514563)
upstream_gene_variant(ENST00000505376)
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
Turic D, 2005(a) C/T P-value=0.69 for pooled genotyping P-value=0.69 for pooled genotyping not significantly associated with ADHD not significantly associated with ADHD Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs930072 (count: 0) View in gBrowse (chr5:36666071..36666071 )