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

SNP Report

Basic Info
Name rs10861968 dbSNP Ensembl
Location chr12:79784553(Fwd)
Variant Alleles G/A
Ancestral Allele A
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000550268; ENST00000553165)
intron_variant(ENST00000261205; ENST00000393240; ENST00000457153; ENST00000549527; ENST00000552744)
nc_transcript_variant(ENST00000549527)
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
Guan L, 2009 single SNP association analyses: Nominal P-value=0.046, Empi...... single SNP association analyses: Nominal P-value=0.046, Empirical P-value=0.274 for ADHD-C More... non-significant for ADHD, but achieve nominal significance f...... non-significant for ADHD, but achieve nominal significance for ADHD-C More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs10861968 (count: 29) View in gBrowse (chr12:79777844..79811286 )
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: 29)