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

SNP Report

Basic Info
Name rs17641078 dbSNP Ensembl
Location chr9:1056959(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; missense_variant.
Polyphen Annotation: possibly damaging(ENST00000302441; ENST00000358146; ENST00000382251)
SIFT Annotation: deleterious(ENST00000302441; ENST00000358146; ENST00000382251)
Consequence to Transcript 3_prime_UTR_variant(ENST00000259622; ENST00000382255)
downstream_gene_variant(ENST00000412350)
missense_variant(ENST00000302441; ENST00000358146; ENST00000382251)
No. of Studies 1 (significant: 0; non-significant: 0; trend: 1)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Lasky-Su J, 2008 P-value=4.73E-06 under Additive model for FBAT-PC HI symptom...... P-value=4.73E-06 under Additive model for FBAT-PC HI symptoms; P-value=8.44E-06 under Dominant model for FBAT-PC HI symptoms More... association finding with P-value association finding with P-value Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs17641078 (count: 0) View in gBrowse (chr9:1056959..1056959 )