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

SNP Report

Basic Info
Name rs1245769 dbSNP Ensembl
Location Chr12:79776101(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000261205; ENST00000457153; ENST00000393240; ENST00000549527; ENST00000552744)
nc_transcript_variant(ENST00000549527)
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
Brookes KJ, 2005 (b) MRM P-value=0.09, Case-control P-value=0.23, TDT P-value=0.7...... MRM P-value=0.09, Case-control P-value=0.23, TDT P-value=0.73 More... was not significant in both TDT analysis and case-control an...... was not significant in both TDT analysis and case-control analysis More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1245769 (count: 17) View in gBrowse (chr12:79760388..79802302 )
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: 17)