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

SNP Report

Basic Info
Name rs2020936 dbSNP Ensembl
Location chr17:28550814(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000261707; ENST00000394821; ENST00000401766)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Ilott NE, 2010 QTDT AT P-value=0.27, X2=1.24, df=1, QTDT AW P-va...... QTDT AT P-value=0.27, X2=1.24, df=1, QTDT AW P-value=0.17, X2=1.92, df=1 at age 2; QTDT AT P-value=0.4, X2=1.34, df=1, QTDT AW P-value=0.27, X2=1.2, df=1 at age 3 More... no significant association no significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2020936 (count: 7) View in gBrowse (chr17:28455538..28552773 )
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)