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

SNP Report

Basic Info
Name rs7782412 dbSNP Ensembl
Location chr7:114290415(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript downstream_gene_variant(ENST00000378237)
intron_variant(ENST00000350908; ENST00000360232; ENST00000390668; ENST00000393489; ENST00000393491; ENST00000393494; ENST00000393498; ENST00000393500; ENST00000403559; ENST00000408937; ENST00000412402; ENST00000441290)
NMD_transcript_variant(ENST00000412402; ENST00000441290)
upstream_gene_variant(ENST00000607845)
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
Ribases, M., 2012 P-value=0.327 in 643 adult attention-deficit/hyperactivity d...... P-value=0.327 in 643 adult attention-deficit/hyperactivity disorder patients and and 619 unrelated controls from Germany; P-value=0.272, OR (95% CI)=- in 431 combined attention-deficit/hyperactivity disorder patients and 619 unrelated controls from Germany More... No significant association was found. No significant association was found. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs7782412 (count: 5) View in gBrowse (chr7:114159875..114290415 )
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: 5)