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

SNP Report

Basic Info
Name rs616668 dbSNP Ensembl
Location chr12:111974280(Fwd)
Variant Alleles T/G
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000377617; ENST00000389153; ENST00000392645; ENST00000471866; ENST00000483311; ENST00000535949; ENST00000542287; ENST00000548492; ENST00000549455; ENST00000550104; ENST00000608853)
nc_transcript_variant(ENST00000392645; ENST00000471866; ENST00000549455)
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/T G P=0.00000862, OR=1.38, 95% CI=1.20-1.59 P=0.00000862, OR=1.38, 95% CI=1.20-1.59 One of the top 24 independent SNP in this ADHD GWAS. One of the top 24 independent SNP in this ADHD GWAS. Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs616668 (count: 48) View in gBrowse (chr12:111844218..112158966 )
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: 48)