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

SNP Report

Basic Info
Name rs169806 dbSNP Ensembl
Location chr11:18059292(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000250018; ENST00000341556; ENST00000417164; ENST00000528338)
NMD_transcript_variant(ENST00000417164)
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
Johansson S, 2010 logistic regression P-value=0.47, OR=1.07 logistic regression P-value=0.47, OR=1.07 no significant association no significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs169806 (count: 39) View in gBrowse (chr11:17942831..18073142 )
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: 39)