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

SNP Report

Basic Info
Name rs1473666 dbSNP Ensembl
Location chrX:7066051(Fwd)
Variant Alleles A/C
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000582827)
intron_variant(ENST00000381077; ENST00000412827; ENST00000424830; ENST00000486446; ENST00000498474; ENST00000540122)
nc_transcript_variant(ENST00000498474)
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
Brookes KJ, 2010 TDT P-value=0.05, OR=1.17 TDT P-value=0.05, OR=1.17 significant evidence for association, but cannot survive str...... significant evidence for association, but cannot survive stringent correction for multiple testing More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 2)


SNPs in LD with rs1473666 (count: 87) View in gBrowse (chrX:6894882..7236970 )
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: 87)