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

SNP Report

Basic Info
Name rs1558902 dbSNP Ensembl
Location chr16:53803574(Fwd)
Variant Alleles T/A
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000394647; ENST00000464071; ENST00000471389; ENST00000570395)
nc_transcript_variant(ENST00000570395)
NMD_transcript_variant(ENST00000464071)
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=0.56, corrected P-value=1, OR=1.05; Assoc...... ADHD risk, P-value=0.56, corrected P-value=1, OR=1.05; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.99, hyperactivity/impulsivity P-value=0.97 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 rs1558902 (count: 37) View in gBrowse (chr16:53799507..53845487 )
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: 37)