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

SNP Report

Basic Info
Name rs17023218 dbSNP Ensembl
Location chr3:29342717(Fwd)
Variant Alleles C/A
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000273139; ENST00000383766; ENST00000383767; ENST00000396583; ENST00000434693; ENST00000445033; ENST00000452462; ENST00000456853; ENST00000471426)
nc_transcript_variant(ENST00000471426)
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
Mick E, 2010 A TDT P-value=1.88E-05 (OR=0.68) TDT P-value=1.88E-05 (OR=0.68) One of the top 20 associations from genome-wide association ...... One of the top 20 associations from genome-wide association results More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs17023218 (count: 3) View in gBrowse (chr3:29338610..29347180 )
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: 3)