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

SNP Report

Basic Info
Name rs362562 dbSNP Ensembl
Location chr20:10243186(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000254976; ENST00000304886; ENST00000421143; ENST00000430336; ENST00000453544)
nc_transcript_variant(ENST00000421143; ENST00000453544)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hawi, Z.,2013 G allelic:T=172,NT=138 ,X2=3.72 ,P-value=0.0535 ,...... G allelic:T=172,NT=138 ,X2=3.72 ,P-value=0.0535 ,EP-value=0.41,OR=1.25 More... TDT analyses of this SNP showed no significant nominal assoc...... TDT analyses of this SNP showed no significant nominal association with ADHD More... Non-significant
Kim JW, 2007 G/A A Single marker analysis FBAT P-value=1; Exploratory analyses ...... Single marker analysis FBAT P-value=1; Exploratory analyses FBAT P-value=0.896 for co-morbid CD, P-value=0.356 for co-morbid MDD, P-value=0.764 for co-morbid BD More... No association was found between ADHD or co-morbidities of A...... No association was found between ADHD or co-morbidities of ADHD and this SNP More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs362562 (count: 7) View in gBrowse (chr20:10236231..10253082 )
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: 7)