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

SNP Report

Basic Info
Name rs1801253 dbSNP Ensembl
Location chr10:115805056(Fwd)
Variant Alleles G/C
Ancestral Allele C
Functional Annotation missense_variant.
Polyphen Annotation: benign(ENST00000369295)
SIFT Annotation: tolerated(ENST00000369295)
Consequence to Transcript missense_variant(ENST00000369295)
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
Hawi, Z., 2012 C:G C P-value=0.9397, X2=0.01, OR=1.01, 95% CI=0.75-1.3...... P-value=0.9397, X2=0.01, OR=1.01, 95% CI=0.75-1.36 More... The marker did not show significant association with ADHD. The marker did not show significant 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 rs1801253 (count: 3) View in gBrowse (chr10:115789375..115805056 )
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: 3)