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

SNP Report

Basic Info
Name rs790531 dbSNP Ensembl
Location chr13:50725514(Fwd)
Variant Alleles A/G
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000461527; ENST00000463474; ENST00000467721; ENST00000468168; ENST00000468522; ENST00000476738; ENST00000486895; ENST00000490577; ENST00000491341; ENST00000491615)
nc_transcript_variant(ENST00000461527; ENST00000463474; ENST00000467721; ENST00000468168; ENST00000468522; ENST00000476738; ENST00000486895; ENST00000490577; ENST00000491341; ENST00000491615)
No. of Studies 1 (significant: 0; non-significant: 0; trend: 1)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Stergiakouli E., 2012 G/A G P=0.000015, OR=1.62, 95% CI=1.30-2.02 P=0.000015, OR=1.62, 95% CI=1.30-2.02 One of the top 31 independent SNP in this ADHD GWAS. One of the top 31 independent SNP in this ADHD GWAS. Trend

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs790531 (count: 22) View in gBrowse (chr13:50532130..50734294 )
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: 22)