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

SNP Report

Basic Info
Name rs553668 dbSNP Ensembl
Location chr10:112839579(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation 3_prime_UTR_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000280155)
No. of Studies 3 (significant: 1; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 3)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
de Cerqueira CC, 2011 C/T chi-square test P-value=0.194, X2=1.687 for allel...... chi-square test P-value=0.194, X2=1.687 for allele frequencies; chi-square test P-value=0.206, X2=3.158 for genotype frequencies More... no significant differences in allele and genotype frequencie...... no significant differences in allele and genotype frequencies were found between patients and controls in this study More... Non-significant
Park L, 2005 C/T TDT P-value=0.033, X2=4.57, RR=3.67 for T allele ...... TDT P-value=0.033, X2=4.57, RR=3.67 for T allele in ADHD-CTDT P-value=0.37, X2=0.82, RR=1.75 for T allele in ADHD-PITDT P-value=0.028, X2=4.84, RR=2.57 for T allele in ADHD-(C+PI) More... revealed a significant association with the ADHD combined su...... revealed a significant association with the ADHD combined subtype and combined and primarily inattentive subtypes considered together More... Significant
Gizer IR, 2009 Meta-analysis model: Random: OR=0.94, 95% CI=0.66-1.34, P-va...... Meta-analysis model: Random: OR=0.94, 95% CI=0.66-1.34, P-value=0.638; Q-statistic: P-value=0.044, I2=63 More... no evidence to suggest an association between this polymorph...... no evidence to suggest an association between this polymorphisms and ADHD More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs553668 (count: 4) View in gBrowse (chr10:112657207..112839579 )
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: 4)