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

SNP Report

Basic Info
Name rs3025873 dbSNP Ensembl
Location chr20:10269040(Fwd)
Variant Alleles G/C
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000254976; ENST00000304886; ENST00000421143; ENST00000430336; ENST00000453544)
nc_transcript_variant(ENST00000421143; ENST00000453544)
No. of Studies 1 (significant: 1; non-significant: 0; 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 G/C C Single marker analysis FBAT P-value=1; Exploratory analyses ...... Single marker analysis FBAT P-value=1; Exploratory analyses FBAT P-value=0.723 for co-morbid CD, P-value=0.021 for co-morbid MDD, P-value=0.952 for co-morbid BD More... Exploratory analysis showed evidence of significant associat...... Exploratory analysis showed evidence of significant association with ADHD and co-morbid MDD More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs3025873 (count: 13) View in gBrowse (chr20:10247685..10280439 )
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: 13)