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

SNP Report

Basic Info
Name rs6565113 dbSNP Ensembl
Location chr16:83107646(Fwd)
Variant Alleles G/T
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000268613; ENST00000428848; ENST00000431540; ENST00000446376; ENST00000539548; ENST00000565636; ENST00000566620; ENST00000569454)
nc_transcript_variant(ENST00000569454)
NMD_transcript_variant(ENST00000539548)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Lasky-Su J, 2008 PBAT P-value=0.005, power ranking=1 within all symptoms phen...... PBAT P-value=0.005, power ranking=1 within all symptoms phenotype in additive model More... achieved significance within a phenotype using the PBAT scre...... achieved significance within a phenotype using the PBAT screening algorithm with various quantitative phenotypes More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs6565113 (count: 15) View in gBrowse (chr16:83106301..83136478 )
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: 15)