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

SNP Report

Basic Info
Name rs3810291 dbSNP Ensembl
Location chr19:47569003(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation 3_prime_UTR_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000253048; ENST00000601973)
nc_transcript_variant(ENST00000594019)
non_coding_exon_variant(ENST00000594019)
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=0.98, corrected P-value=1, OR=1; Associat...... ADHD risk, P-value=0.98, corrected P-value=1, OR=1; Association to ADHD subphenotypes in the German sample, inattention, P-value=1, hyperactivity/impulsivity P-value=0.57 More... No significant association was reported in this study. No significant association was reported in this study. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs3810291 (count: 14) View in gBrowse (chr19:47569003..47611128 )
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: 14)