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

SNP Report

Basic Info
Name rs1786581 dbSNP Ensembl
Location chr18:11852182(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000526991)
downstream_gene_variant(ENST00000609238)
intron_variant(ENST00000269162; ENST00000334049; ENST00000423027; ENST00000535121; ENST00000585642; ENST00000586474; ENST00000590228)
nc_transcript_variant(ENST00000586474)
upstream_gene_variant(ENST00000588284)
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
Laurin N, 2008(b) C/T TDT P-value=0.384, X2=0.758 TDT P-value=0.384, X2=0.758 no significant evidence of association no significant evidence of association Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs1786581 (count: 0) View in gBrowse (chr18:11852182..11852182 )