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

SNP Report

Basic Info
Name rs6919857 dbSNP Ensembl
Location chr6:137140454(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation upstream_gene_variant.
Consequence to Transcript upstream_gene_variant(ENST00000318471; ENST00000367756; ENST00000541292)
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
Lantieri F, 2010 C:T Binomial P-value=0.62, OR=1.03 for whole sample; Binomial P-...... Binomial P-value=0.62, OR=1.03 for whole sample; Binomial P-value=0.55, OR=1.01 for C-subtype More... no significant association no significant association Non-significant
Neale BM, 2008 C:T Uncorrected TDT P-value=2.46E-05 (OR=0.749); Corrected TDT P...... Uncorrected TDT P-value=2.46E-05 (OR=0.749); Corrected TDT P-value=4.79E-05 (OR=0.749) More... One of top 25 results in both uncorrected and corrected TDT ...... One of top 25 results in both uncorrected and corrected TDT test More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 1)


SNPs in LD with rs6919857 (count: 58) View in gBrowse (chr6:137083138..137243020 )
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: 58)