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

SNP Report

Basic Info
Name rs192303 dbSNP Ensembl
Location chr16:55700224(Fwd)
Variant Alleles C/G
Ancestral Allele C
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000568529; ENST00000568655; 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
Sengupta, S. M., 2012 G/C P-value=0.27, Z statistic (allele 1)=1.11 P-value=0.27, Z statistic (allele 1)=1.11 No significant association was found in this study. No significant association was found in this study. Non-significant
Kim JW, 2008 X2=0.896, P-value=0.343, OR=1.1 X2=0.896, P-value=0.343, OR=1.1 not associated with ADHD not associated with ADHD Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs192303 (count: 11) View in gBrowse (chr16:55669681..55704795 )
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: 11)