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

SNP Report

Basic Info
Name rs36017 dbSNP Ensembl
Location chr16:55718818(Fwd)
Variant Alleles G/C
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000567238; ENST00000568529; ENST00000568943)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hawi, Z., 2012 C:G G P-value=0.792, X2=0.07, OR=1.04, 95% CI=0.80-1.33 P-value=0.792, X2=0.07, OR=1.04, 95% CI=0.80-1.33 The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant
Sengupta, S. M., 2012 C/G P-value=0.13, Z statistic (allele 1)=¨C1.53 P-value=0.13, Z statistic (allele 1)=¨C1.53 No significant association was found in this study. No significant association was found 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 rs36017 (count: 6) View in gBrowse (chr16:55718818..55726462 )
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: 6)