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

SNP Report

Basic Info
Name rs1801133 dbSNP Ensembl
Location chr1:11856378(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation downstream_gene_variant; missense_variant.
Polyphen Annotation: probably damaging(ENST00000376583; ENST00000376585; ENST00000376590; ENST00000376592)
SIFT Annotation: deleterious(ENST00000376583; ENST00000376585) | tolerated(ENST00000376590; ENST00000376592)
Consequence to Transcript downstream_gene_variant(ENST00000418034)
missense_variant(ENST00000376583; ENST00000376585; ENST00000376590; ENST00000376592)
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
Ergul, E., 2012 C/T allelic P-value=0.425, X2=1.711, df=2; genotypic ...... allelic P-value=0.425, X2=1.711, df=2; genotypic P-value=0.204, X2=1.613, df=1, OR (95% CI)=0.745 (0.473-1.174) for CC; P-value=0.351, X2=0.870, df=1, OR (95% CI)=1.242 (0.788-1.957) for CT; P-value=0.511, X2=0.432, df=1, OR (95% CI)=1.314 (0.581-2.991) for TT More... There were no significant allele or genotype differences bet...... There were no significant allele or genotype differences between cases and controls. More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1801133 (count: 0) View in gBrowse (chr1:11856378..11856378 )