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

SNP Report

Basic Info
Name rs4929949 dbSNP Ensembl
Location chr11:8604593(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000315204; ENST00000358872; ENST00000396672; ENST00000396673; ENST00000418597; ENST00000422559; ENST00000431279; ENST00000454443; ENST00000526517; ENST00000532336; ENST00000534493)
nc_transcript_variant(ENST00000526517; ENST00000532336)
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=0.42, corrected P-value=1, OR=0.93; Assoc...... ADHD risk, P-value=0.42, corrected P-value=1, OR=0.93; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.5, hyperactivity/impulsivity P-value=0.3 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 rs4929949 (count: 55) View in gBrowse (chr11:8413870..8682465 )
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: 55)