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

SNP Report

Basic Info
Name rs347405 dbSNP Ensembl
Location chr13:42790179(Fwd)
Variant Alleles C/G
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000261491; ENST00000337343; ENST00000379274; ENST00000489851; ENST00000498255; ENST00000536612; ENST00000538674; ENST00000540693)
nc_transcript_variant(ENST00000489851; ENST00000498255)
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
Weber H, 2011 C/G Nominal P-value=0.043, Bonferroni P-value=0.987 Nominal P-value=0.043, Bonferroni P-value=0.987 significantly associated with ADHD but was not significant f...... significantly associated with ADHD but was not significant following Bonferroni correction More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs347405 (count: 2) View in gBrowse (chr13:42704669..42798106 )
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: 2)