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

SNP Report

Basic Info
Name rs1805066 dbSNP Ensembl
Location chr16:55719143(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation missense_variant.
Polyphen Annotation: benign(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000567238; ENST00000568529; ENST00000568943)
SIFT Annotation: tolerated(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000567238; ENST00000568529; ENST00000568943)
Consequence to Transcript missense_variant(ENST00000219833; ENST00000379906; ENST00000414754; ENST00000561820; ENST00000566163; ENST00000567238; ENST00000568529; ENST00000568943)
No. of Studies 1 (significant: 0; non-significant: 0; trend: 1)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hahn MK, 2009 G:A non-synonymous SNP in coding region of candidate gene SLC6A2 non-synonymous SNP in coding region of candidate gene SLC6A2 Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1805066 (count: 0) View in gBrowse (chr16:55719143..55719143 )