ADHDgene Database
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Type:
  • Large-scale studies
  • Data Summary
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

SNP Report

Basic Info
Name rs7999483 dbSNP Ensembl
Location Chr13:36353437(Fwd)
Variant Alleles A/C
Ancestral Allele A
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000379893; ENST00000360631; ENST00000255448)
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
Havik, B., 2012 P-value=0.189, OR (95% CI)=0.82 (0.62-1.09) in the Norwegian...... P-value=0.189, OR (95% CI)=0.82 (0.62-1.09) in the Norwegian sample; P-value=0.287, OR (95% CI)=1.20 (0.96-1.51) in the German sample; P-value=0.809, OR (95% CI)=1.03 (0.87-1.23) in the merged sample 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 rs7999483 (count: 13) View in gBrowse (chr13:36308757..36383264 )
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: 1)

LD-proxies (count: 12)

Copyright: Bioinformatics Lab, Institute of Psychology, Chinese Academy of Sciences Feedback
Last update: Feb 26, 2014