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

SNP Report

Basic Info
Name rs9608617 dbSNP Ensembl
Location chr22:27906244(Fwd)
Variant Alleles G/C
Ancestral Allele G
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
Neale BM, 2008 C:G Uncorrected TDT P-value=3.29E-05 (OR=1.376); Corrected TDT P...... Uncorrected TDT P-value=3.29E-05 (OR=1.376); Corrected TDT P-value=2.96E-05 (OR=1.376) More... One of top 25 results in both uncorrected and corrected TDT ...... One of top 25 results in both uncorrected and corrected TDT test More... Non-significant
Lantieri F, 2010 C:G Binomial P-value=0.86, OR=0.89 for whole sample; Binomial P-...... Binomial P-value=0.86, OR=0.89 for whole sample; Binomial P-value=0.91, OR=0.84 for C-subtype More... no significant association no significant association Non-significant

SNP related genes (count: 0)

SNPs in LD with rs9608617 (count: 6) View in gBrowse (chr22:27903420..27913387 )
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)