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

SNP Report

Basic Info
Name rs4765913 dbSNP Ensembl
Location chr12:2419896(Fwd)
Variant Alleles A/T
Ancestral Allele T
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000327702; ENST00000335762; ENST00000344100; ENST00000347598; ENST00000399591; ENST00000399595; ENST00000399597; ENST00000399601; ENST00000399603; ENST00000399606; ENST00000399617; ENST00000399621; ENST00000399629; ENST00000399634; ENST00000399637; ENST00000399638; ENST00000399641; ENST00000399644; ENST00000399649; ENST00000399655; ENST00000402845; ENST00000406454; ENST00000480911; LRG_334t1; LRG_334t2; LRG_334t3; LRG_334t4)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Schimmelmann, B. G.,2013 Nominal two-sided P-value=0.937 (OR=1.01;95%CI=0.83-1.22) Nominal two-sided P-value=0.937 (OR=1.01;95%CI=0.83-1.22) No evidence for association was found with ADHD for the rema...... No evidence for association was found with ADHD for the remaining eight SNPs, which were found to be genome-wide significant for BD in international GWAS More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs4765913 (count: 5) View in gBrowse (chr12:2321820..2420526 )
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: 5)