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

SNP Report

Basic Info
Name rs13317247 dbSNP Ensembl
Location chr3:7026535(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000357716; ENST00000389335; ENST00000389336; ENST00000402647; ENST00000403881; ENST00000435689; ENST00000440923; ENST00000443259; ENST00000448328; ENST00000467425; ENST00000486284)
NMD_transcript_variant(ENST00000389335; ENST00000435689; ENST00000440923; ENST00000443259; ENST00000467425)
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
Yang L, 2013 P-value=0.0000637 P-value=0.0000637 The SNPs associated with P values of 1E-5 or lower The SNPs associated with P values of 1E-5 or lower Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs13317247 (count: 1) View in gBrowse (chr3:7026273..7026535 )
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: 1)