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

SNP Report

Basic Info
Name rs362988 dbSNP Ensembl
Location Chr20:10281370(Fwd)
Variant Alleles G/A
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000421143; ENST00000254976; ENST00000453544; ENST00000495883; ENST00000304886)
nc_transcript_variant(ENST00000421143; ENST00000453544; ENST00000495883)
No. of Studies 3 (significant: 1; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 3)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Guan L, 2009 single SNP association analyses: Nominal P-value=0.033, Empi...... single SNP association analyses: Nominal P-value=0.033, Empirical P-value=0.505 for ADHD-I More... non-significant for ADHD, but achieve nominal significance f...... non-significant for ADHD, but achieve nominal significance for ADHD-I More... Significant
Sarkar, K., 2012 A/G allelic P-value=0.31, X2=1.01 for case-control, P...... allelic P-value=0.31, X2=1.01 for case-control, P-value=0.47, X2=0.52 for family-based; genotypic P-value=0.47, X2=1.49 for case-control, P-value=0.59, X2=1.04 for family-based; X2=1.5, TDT P-value=0.22, Relative risk (95% CI)=0.6 (0.35¨C1.1) More... Case-control analysis revealed lack of any significant diffe...... Case-control analysis revealed lack of any significant difference in allelic frequencies between ADHD probands, their parents and controls P>0.05. rs362988 'G' allele showed a bias in transmission though the difference was statistically insignificant. More... Non-significant
Nyman ES, 2007 No available information. No available information. No evidence of association was seen. No evidence of association was seen. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs362988 (count: 1) View in gBrowse (chr20:10281370..10282027 )
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: 1)