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

SNP Report

Basic Info
Name rs2073837 dbSNP Ensembl
Location chr9:136522928(Fwd)
Variant Alleles G/A
Ancestral Allele A
Functional Annotation intron_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000393056)
upstream_gene_variant(ENST00000425189)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Nyman ES, 2007 Logistic regression for single markers: adjusted for sex: P-...... Logistic regression for single markers: adjusted for sex: P-value=0.0055, OR=2.69, 95%CI=1.34-5.43 for 22vs.11, P-value=0.0099, OR=0.44, 95%CI=0.23-0.82 for 11/12vs.22; Males: P-value=0.0027, OR=5.05, 95%CI=1.75-14.54 for 22vs.11, P-value=0.0036, OR=0.22, 95%CI=0.08-0.61 for 11/12vs.22 More... The minor homozygote was risk conferring compared with the m...... The minor homozygote was risk conferring compared with the major homozygote adjusted for sex and an even stronger effect was seen in males More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs2073837 (count: 6) View in gBrowse (chr9:136522187..136532183 )
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)