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

SNP Report

Basic Info
Name rs10421632 dbSNP Ensembl
Location chr19:57764770(Fwd)
Variant Alleles G/A
Functional Annotation missense_variant.
Polyphen Annotation: benign(ENST00000354309; ENST00000414468; ENST00000535550)
SIFT Annotation: tolerated(ENST00000354309; ENST00000414468; ENST00000535550)
Consequence to Transcript missense_variant(ENST00000354309; ENST00000414468; ENST00000535550)
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
Lasky-Su J, 2008 P-value=9.68E-06 under Additive model for HI symptom count P-value=9.68E-06 under Additive model for HI symptom count association finding with P-value association finding with P-value Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs10421632 (count: 27) View in gBrowse (chr19:57717532..57779521 )
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: 27)