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

SNP Report

Basic Info
Name rs16917204 dbSNP Ensembl
Location chr11:27668355(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000499008; ENST00000499568; ENST00000500662; ENST00000501176; ENST00000502161; ENST00000530313; ENST00000530686; ENST00000532965)
nc_transcript_variant(ENST00000499008; ENST00000499568; ENST00000500662; ENST00000501176; ENST00000502161; ENST00000530313; ENST00000530686; ENST00000532965)
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
Cho SC, 2010(a) allelic P-value=0.726, X2 (1df)=0.123, genotypic ...... allelic P-value=0.726, X2 (1df)=0.123, genotypic P-value=0.913, X2 (2df)=0.181 in boys; allelic P-value=0.524, X2 (1df)=0.407, genotypic P-value=0.766, X2 (2df)=0.533 in girls More... no significant association no significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 1)


SNPs in LD with rs16917204 (count: 0) View in gBrowse (chr11:27668355..27668355 )