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

SNP Report

Basic Info
Name rs760609 dbSNP Ensembl
Location chr6:114708100(Fwd)
Variant Alleles A/C
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000518470)
nc_transcript_variant(ENST00000518470)
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
Mick E, 2010 A TDT P-value=2.51E-05 (OR=1.37) TDT P-value=2.51E-05 (OR=1.37) One of the top 20 associations from genome-wide association ...... One of the top 20 associations from genome-wide association results More... Non-significant

SNP related genes (count: 0)

SNPs in LD with rs760609 (count: 23) View in gBrowse (chr6:114612973..114721697 )
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: 23)