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

SNP Report

Basic Info
Name rs10838881 dbSNP Ensembl
Location chr11:48387275(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation missense_variant.
Polyphen Annotation: possibly damaging(ENST00000319813)
SIFT Annotation: deleterious(ENST00000319813)
Consequence to Transcript missense_variant(ENST00000319813)
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
Hinney, A., 2011 T GWAS P-value=2.24E-05, OR=1.66, Replication FBAT P-value=0.1...... GWAS P-value=2.24E-05, OR=1.66, Replication FBAT P-value=0.1083, Combination P-value=9.29E-06 More... This GWAS in a small group of clinically ascertained young G...... This GWAS in a small group of clinically ascertained young German patients with ADHD and population-based controls did not reveal genome-wide significant findings. Replication attempts in further German and international samples did also not lead to a P-value(s) below 5E-08. More... Trend

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)

SNPs in LD with rs10838881 (count: 43) View in gBrowse (chr11:48199227..48556319 )
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: 43)