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

SNP Report

Basic Info
Name rs2273505 dbSNP Ensembl
Location chr20:61990878(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000370263; ENST00000463705; ENST00000467563; ENST00000498043)
nc_transcript_variant(ENST00000463705; ENST00000467563)
NMD_transcript_variant(ENST00000498043)
upstream_gene_variant(ENST00000370257)
No. of Studies 2 (significant: 1; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Bobb AJ, 2005 allelic TDT P-value=0.71, OR=1.12 in case-control analysis; ...... allelic TDT P-value=0.71, OR=1.12 in case-control analysis; allelic TDT P-value=0.27, RR=1.63 in family-based analysis More... non-significant association non-significant association Non-significant
Lee J, 2008 G/A P-value=0.085, X2 (1df)=2.97 in all subtypes; P-v...... P-value=0.085, X2 (1df)=2.97 in all subtypes; P-value=0.808, X2 (1df)=0.059 in inattentive subtype; P-value=0.033, X2 (1df)=4.568 in combined subtype; P-value=0.026 in FBAT analysis for hyperactive/impulsive symptoms More... nominally significant evidence of association with the ADHD ...... nominally significant evidence of association with the ADHD combined subtype and with teacher-rated hyperactivity-impulsivity scores More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2273505 (count: 0) View in gBrowse (chr20:61990878..61990878 )