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

SNP Report

Basic Info
Name rs60593443 dbSNP Ensembl
Location chr8:26636906(Fwd)
Variant Alleles T/A
Ancestral Allele T
Functional Annotation intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant.
Polyphen Annotation: benign(ENST00000380572)
SIFT Annotation: deleterious(ENST00000380572)
Consequence to Transcript intron_variant(ENST00000276393; ENST00000354550; ENST00000380573; ENST00000380581; ENST00000380582; ENST00000380586; ENST00000380587; ENST00000518621; ENST00000519096; ENST00000519229; ENST00000521711)
missense_variant(ENST00000380572)
nc_transcript_variant(ENST00000518621)
NMD_transcript_variant(ENST00000519096; ENST00000521711)
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
Hawi, Z., 2012 T:A T P-value=0.1129, X2=2.51, OR=1.35, 95% CI=0.93-1.9...... P-value=0.1129, X2=2.51, OR=1.35, 95% CI=0.93-1.94 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 0)


SNPs in LD with rs60593443 (count: 0) View in gBrowse (chr8:26636906..26636906 )