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

SNP Report

Basic Info
Name rs10150332 dbSNP Ensembl
Location chr14:79936964(Fwd)
Variant Alleles T/C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000281127; ENST00000335750; ENST00000428277; ENST00000553803; ENST00000554719; ENST00000554738; ENST00000555073; ENST00000555387; ENST00000556003; ENST00000557594)
nc_transcript_variant(ENST00000553803; ENST00000555073; ENST00000556003)
NMD_transcript_variant(ENST00000554738; ENST00000555387)
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=0.84, corrected P-value=1,OR=0.98; Associ...... ADHD risk, P-value=0.84, corrected P-value=1,OR=0.98; Association to ADHD subphenotypes in the German sample, inattention, P-value=0.83, hyperactivity/impulsivity P-value=0.05 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 rs10150332 (count: 10) View in gBrowse (chr14:79890456..79945162 )
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: 10)