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

SNP Report

Basic Info
Name rs6077699 dbSNP Ensembl
Location chr20:10224306(Fwd)
Variant Alleles A/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: 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 A/C C Single marker analysis FBAT P-value=0.839; Exploratory analy...... Single marker analysis FBAT P-value=0.839; Exploratory analyses FBAT P-value=0.571 for co-morbid CD, P-value=0.412 for co-morbid MDD, P-value=0.73 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: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs6077699 (count: 4) View in gBrowse (chr20:10224306..10233264 )
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)