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

SNP Report

Basic Info
Name rs1049353 dbSNP Ensembl
Location chr6:88853635(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; synonymous_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000362094)
downstream_gene_variant(ENST00000551417)
synonymous_variant(ENST00000369499; ENST00000369501; ENST00000428600; ENST00000468898; ENST00000535130; ENST00000537554; ENST00000549716; ENST00000549890)
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
Lu AT, 2008 A/G P-value>0.05 P-value>0.05 showed no association with ADHD showed no association with ADHD Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1049353 (count: 5) View in gBrowse (chr6:88821736..88853635 )
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)