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

SNP Report

Basic Info
Name rs6327 dbSNP Ensembl
Location chr1:115829986(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000369512; ENST00000425449; LRG_260t1)
nc_transcript_variant(ENST00000425449)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Ribases M, 2008 genotypic P-value=0.036; genotypic P-value=0.44 in dominant ...... genotypic P-value=0.036; genotypic P-value=0.44 in dominant model; genotypic P-value=0.04, OR=1.49 (1.02-2.16) in recessive model; allelic P-value=0.48 in Adults More... provided evidence of association with adulthood ADHD provided evidence of association with adulthood ADHD Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs6327 (count: 4) View in gBrowse (chr1:115809848..115830631 )
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: 4)