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

SNP Report

Basic Info
Name rs6100796 dbSNP Ensembl
Location chr20:58800873(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000421257; ENST00000427820; ENST00000431181; ENST00000432910; ENST00000437035; ENST00000458422)
nc_transcript_variant(ENST00000421257; ENST00000427820; ENST00000431181; ENST00000432910; ENST00000437035; ENST00000458422)
No. of Studies 1 (significant: 0; non-significant: 0; trend: 1)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Neale BM, 2010 (a) T:C P-value=2.03E-05 P-value=2.03E-05 one of top 50 hits from the Genome-Wide Attention-Deficit/Hy...... one of top 50 hits from the Genome-Wide Attention-Deficit/Hyperactivity Disorder (ADHD) meta-analysis More... Trend

SNP related genes (count: 0)

SNPs in LD with rs6100796 (count: 21) View in gBrowse (chr20:58797699..58827268 )
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: 21)