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

SNP Report

Basic Info
Name rs1051730 dbSNP Ensembl
Location chr15:78894339(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; synonymous_variant.
Consequence to Transcript nc_transcript_variant(ENST00000558903)
NMD_transcript_variant(ENST00000559658)
non_coding_exon_variant(ENST00000558903)
synonymous_variant(ENST00000326828; ENST00000348639; ENST00000559658)
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
Thakur G. A., 2012 C/T T FBAT: Z=-1.52, P=0.13, effect size=0.12 FBAT: Z=-1.52, P=0.13, effect size=0.12 No association with ADHD was found. No association with ADHD 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 rs1051730 (count: 44) View in gBrowse (chr15:78724469..79085915 )
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: 44)