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

SNP Report

Basic Info
Name rs2206161 dbSNP Ensembl
Location chr20:10334969(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000421143; ENST00000453544)
nc_transcript_variant(ENST00000421143; ENST00000453544)
upstream_gene_variant(ENST00000446637)
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
Kim JW, 2007 T/C C Single marker analysis FBAT P-value=0.295; Exploratory analy...... Single marker analysis FBAT P-value=0.295; Exploratory analyses FBAT P-value=0.66 for co-morbid CD, P-value=0.265 for co-morbid MDD, P-value=0.283 for co-morbid BD More... No association was found between ADHD or co-morbidities of A...... No association was found between ADHD or co-morbidities of ADHD and this SNP More... Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 2)


SNPs in LD with rs2206161 (count: 4) View in gBrowse (chr20:10334478..10342441 )
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: 4)