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

SNP Report

Basic Info
Name rs2287019 dbSNP Ensembl
Location chr19:46202172(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000591606)
intron_variant(ENST00000012049; ENST00000366382; ENST00000592769)
nc_transcript_variant(ENST00000592769)
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
Albayrak O., 2013 ADHD risk, P-value=1, corrected P-value=n.a.,OR=0.65; Associ...... ADHD risk, P-value=1, corrected P-value=n.a.,OR=0.65; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.51, hyperactivity/impulsivity P-value=0.96 More... No significant association was reported in this study. No significant association was reported in this study. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2287019 (count: 3) View in gBrowse (chr19:46180184..46202172 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 3)