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

SNP Report

Basic Info
Name rs11646411 dbSNP Ensembl
Location chr16:82746937(Fwd)
Variant Alleles C/G
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000268613; ENST00000428848; ENST00000431540; ENST00000446376; ENST00000539548; ENST00000562601; ENST00000565636; ENST00000566333; ENST00000566620; ENST00000567445; ENST00000568770; ENST00000569144; ENST00000569455)
nc_transcript_variant(ENST00000566333; ENST00000569455)
NMD_transcript_variant(ENST00000539548; ENST00000562601; ENST00000568770; ENST00000569144)
No. of Studies 1 (significant: 0; non-significant: 0; trend: 1)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Lesch KP, 2008 ANOVA P-value=7.40E-06, Mean of ranks=79 ANOVA P-value=7.40E-06, Mean of ranks=79 one of the top 30 single SNPs located in gene regions (inclu...... one of the top 30 single SNPs located in gene regions (including 100kb of flanking sequences) ranked according to the mean rank calculated across three statistics; annotated by GWAS Catalog More... Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs11646411 (count: 0) View in gBrowse (chr16:82746937..82746937 )