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 rs2295426 dbSNP Ensembl
Location Chr14:59376455(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000556815; ENST00000555378; ENST00000556026)
nc_transcript_variant(ENST00000556815; ENST00000555378; ENST00000556026)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Lantieri F, 2010 C:T Binomial P-value=0.41, OR=0.97 for whole sample; Binomial P-...... Binomial P-value=0.41, OR=0.97 for whole sample; Binomial P-value=0.44, OR=0.97 for C-subtype More... no significant association no significant association Non-significant
Neale BM, 2008 C:T Corrected TDT P-value=1.00E-05 (OR=0.7103) Corrected TDT P-value=1.00E-05 (OR=0.7103) One of top 25 results in corrected TDT test One of top 25 results in corrected TDT test Non-significant

SNP related genes (count: 0)

SNPs in LD with rs2295426 (count: 43) View in gBrowse (chr14:59329044..59430630 )
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: 42)

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