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

SNP Report

Basic Info
Name rs1386496 dbSNP Ensembl
Location chr12:72350790(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000333850; ENST00000546576)
nc_transcript_variant(ENST00000546576)
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
Sheehan K, 2007 T TDT test: P-value=0.636, OR=0.81 for full trios; P-value=0.8...... TDT test: P-value=0.636, OR=0.81 for full trios; P-value=0.804, OR=0.77 for paternal transmission; P-value=0.839, OR=0.85 for maternal transmission. More... There is no significant difference in the transmission of al...... There is no significant difference in the transmission of alleles to ADHD cases. More... Non-significant
Johansson S, 2010 logistic regression P-value=0.08, OR=1.27, meta-analysis P-v...... logistic regression P-value=0.08, OR=1.27, meta-analysis P-value=0.24, OR=0.89 More... no significant association no significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1386496 (count: 15) View in gBrowse (chr12:72349290..72398117 )
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)