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

SNP Report

Basic Info
Name rs6592952 dbSNP Ensembl
Location chr7:50560255(Fwd)
Variant Alleles C/A
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000380984)
intron_variant(ENST00000357936; ENST00000426377; ENST00000430300; ENST00000431062; ENST00000444124; ENST00000444733)
NMD_transcript_variant(ENST00000444733)
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
Guan L, 2009 single SNP association analyses: Nominal P-value=0.003, Empi...... single SNP association analyses: Nominal P-value=0.003, Empirical P-value=0.032 for ADHD-I More... non-significant for ADHD, but achieve nominal and empirical ...... non-significant for ADHD, but achieve nominal and empirical significance for ADHD-I More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs6592952 (count: 31) View in gBrowse (chr7:50533539..50573848 )
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: 31)