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

SNP Report

Basic Info
Name rs591556 dbSNP Ensembl
Location Chr11:18061400(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation NMD_transcript_variant; intron_variant.
Consequence to Transcript NMD_transcript_variant(ENST00000417164)
intron_variant(ENST00000250018; ENST00000341556; ENST00000417164; ENST00000528338)
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=0.74, OR=0.96 logistic regression P-value=0.74, OR=0.96 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 rs591556 (count: 9) View in gBrowse (chr11:17945020..18063977 )
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: 1)

LD-proxies (count: 8)