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

SNP Report

Basic Info
Name rs362986 dbSNP Ensembl
Location chr20:10277034(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript downstream_gene_variant(ENST00000430336)
intron_variant(ENST00000254976; ENST00000304886; ENST00000421143; ENST00000453544)
nc_transcript_variant(ENST00000421143; ENST00000453544; ENST00000495883)
non_coding_exon_variant(ENST00000495883)
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
Feng Y, 2005(b) T/C allelic TDT P-value=0.336, X2=0.925 in Irvine sam...... allelic TDT P-value=0.336, X2=0.925 in Irvine sample; allelic TDT P-value=0.112, X2=2.532 in Toronto sample More... there was no significant result both in the Toronto sample a...... there was no significant result both in the Toronto sample and the Irvine sample More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs362986 (count: 0) View in gBrowse (chr20:10277034..10277034 )