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

SNP Report

Basic Info
Name rs1386497 dbSNP Ensembl
Location chr12:72392290(Fwd)
Variant Alleles C/A
Ancestral Allele A
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000333850)
No. of Studies 2 (significant: 1; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Manor I, 2008 P-value>0.05 P-value>0.05 no significant association no significant association Non-significant
Sheehan K, 2005 A/C allelic TDT P-value=0.048, X2=4.2, OR=1.45; TDT P...... allelic TDT P-value=0.048, X2=4.2, OR=1.45; TDT P-value=0.3, X2=0.75, OR=1.4 of paternal origin; TDT P-value=0.06, X2=4.1, OR=1.8 of maternal origin More... a weaker association was observed a weaker association was observed Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs1386497 (count: 16) View in gBrowse (chr12:72349290..72404378 )
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: 16)