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

SNP Report

Basic Info
Name rs2952151 dbSNP Ensembl
Location chr17:37828496(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000300658; ENST00000378011; ENST00000579146)
downstream_gene_variant(ENST00000269582; ENST00000394246; ENST00000429199; ENST00000577337; ENST00000580898; ENST00000581428; ENST00000582276; ENST00000584620)
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
Hawi, Z., 2012 C:T C P-value=0.7217, X2=0.13, OR=1.05, 95% CI=0.79-1.3...... P-value=0.7217, X2=0.13, OR=1.05, 95% CI=0.79-1.38 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)

SNPs in LD with rs2952151 (count: 43) View in gBrowse (chr17:37770005..37884037 )
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: 43)